Log in

Job Postings

If you're looking for a rewarding career in the manufacturing industry with ongoing opportunity for career growth and a competitive salary keep checking back to view new openings in the Tampa Bay Area.

As a BAMA member, you are able to post job openings here by logging into your online BAMA account and clicking "Add Post". 
You can also email the job description along with complete contact info to admin@bama-fl.org. Please include any preferred certifications for the job.
If not a member of BAMA, please consider joining - here is a link to our application.

Job Seekers
- please pay attention to the date posted as some jobs may be closed. 

  • February 14, 2019 9:01 PM | Anonymous member (Administrator)


    Overview

    Daily activities include support of utilities, facility, HVAC, and outside contracts that include: Pest Control, Security, landscaping, cafeteria services and site services; overall operation of the utility equipment. Assure that Facility/Utility related work orders, PM’s, critical system work orders are executed and completed. Oversee the passivation, preventative maintenance, shutdowns, department metrics, and training programs for department associates. Support Reliability Program.

    Responsibilities

    Support the Facility Review Board (FRB) process. 

    Leads and ensures on time completion of compliance investigations, non-conformances, deviations, CAPAs, and work orders.

    Facility and Utility departments and oversee operation, installation, and maintenance of related equipment.

    Respond to emergencies 24/7, work with the hurricane preparedness team and Coordinate Security services during facility emergencies.

    Assist validation on protocols, revalidation, review and sign-off. Assist on validation on protocols related to Utility department.

    Participating in inspections conducted by internal and external regulators and contract customers.

    Ensures compliance with EHS&S and OSHA requirements.

    Assist FM Global and EHS on liability and risk assessments.

    Support projects as needed, including document review, vendor negotiations, etc.

    Work with various state and local agencies, FDA, ETA, etc.

    Communicate with contractors on projects, contract negotiations, scheduling and compliance with company policies.

    Support activities for outside contractors for Site services, Security, landscaping, pest control, and cafeteria service to ensure they stay compliant with site and contract.

    Support the site reliability program.

    Support requests for computerized security system, as well as digital media, cameras, and intrusion systems.

    Scope of Position:

    Support activities for utility, facility, HVAC, site, security, landscaping, pest control, cafeteria services, overall operation of the utility and facility equipment. Assure that facility, utility related work orders, PM’s, critical system work orders are executed and completed.

    Qualifications

    BA Degree in Mechanical Engineering, Business or Maintenance related field. Background in Maintenance Reliability a plus.

    Logical approach to problem solving. Good organizational skills, able to work quickly and under pressure. Good verbal and written communication skills. Must be detailed and safety oriented and quality conscious.

    Project Management and leadership abilities. Computer skills with Microsoft Office a plus, and various tools. Utility computer monitoring systems, such as a BAS, EMS or BMS systems.

    5-10 years maintenance/utilities experience.  Position includes responsibility over associates to provide assistance withtroubleshooting  industrial process equipment. Pharmaceutical or food industry experience a plus.

    Apply Here:  www.bauschhealth.com/careers

  • February 14, 2019 8:58 PM | Anonymous member (Administrator)


    Overview

    To provide leadership in the Compounding Department for all personnel to ensure that quality products are manufactured to meet the production plan. Place customer service and accountability to the customer as the constant goal. Coordinate closely with other departments on operational and planning issues related to meeting the production plans and company goals. Assume responsibility for the GMP, environmental health and safety procedure awareness and compliance within the respective area.

    Responsibilities

    • Supervise, develop, provide feedback and coach employees. Complete performance reviews semi-annually.
    • Review weekly production schedule and work with the Planning department on capacity and scheduling issues. Coordinate activities to support the production schedule. Participate in process related issues using thorough technical process knowledge.
    • Perform investigations and write reports as required.
    • Review, approve, write and revise SOP's and other documentation.
    • Participate and lead in Operational Excellence projects and attend GMP training sessions as required. Train/re-train department personnel on safety, cGMPs and SOPs as needed. Work with Tech Services, R&D and Contract Manufacturing on the transfer of new products & engineering studies. Perform audits of area on scheduled basis for compliance to procedures. 
    • Asset and supply management. Generate required WOs and POs.
    • Operate department within budget guidelines. Review standards annually for necessary revisions.

    Qualifications

    BS in Science/Technical field; Chemistry, Biology or Engineering. Can be augmented with years of experience in sterile pharmaceuticals.  Demonstrated exceptional people management and leadership 

    Apply Here:  www.bauschhealth.com/careers

  • February 14, 2019 8:45 PM | Anonymous member (Administrator)


    Manage proper Inventory levels and supply flow for assigned commodities, activity requires close working relationship with procurement, shop floor planning and quality. Provide overall obsolescence analysis on monthly basis.  Provide ERP system maintenance activities. 

    Responsibilities

    1.       Inventory analysis and requisitioning to procurement for assigned commodities insuring material availability while minimizing inventory and obsolescence exposure.

    2.       Insure material receipts are processed and released in a timely fashion to support manufacturing needs.

    3.       Works closely with shop floor planning and incoming quality inspection.

    4.       Provide ERP system maintenance

    5.       Supports commodity material changes to specification and material/supplier transitions.

    6.       Responsibility for overall obsolescence planning and management on monthly basis. Forecasting potential obsolescence for future periods.

    This position will require electronic planning system knowledge to provide maintenance of these systems for inventory planning and requisitioning of materials

    This role will have planning responsibilities managing internal customer needs against supply capabilities insuring a high level of customer service while staying within inventory targeted ranges.  Will work closely with finance for management of obsolescence. 

    This position will work closing with shop floor planning and Quality expediting materials as needed.

    Qualifications

    BS in Logistics, Business or Management Sciences, Excellent communication skills throughout all levels of the organization. Detail oriented with very good organizational skills. Computerized MRP systems, MS office products with emphasis on Excel. Some knowledge of change control management.

    APICS certification preferred

    5-10 years of supply chain experience in pharmaceuticals or other process related industry.

    Apply Here:  www.bauschhealth.com/careers 

  • February 14, 2019 8:42 PM | Anonymous member (Administrator)

    Valeant Pharmaceuticals International, Inc. is a diverse pharmaceutical company that is committed to focusing on our key stakeholders while delivering consistently high performance. Our values provide the overall direction for our company, and provide us with the tools necessary to rise to any challenge by leveraging our collective hard work and effort along with our unwavering competitive spirit. These values help us set goals based on our organization’s potential and what we hope it will become.

    The Manager of Aseptic Process Engineering is responsible for leadership of the engineering competency for US Pharmaceutical manufacturing and executing projects that align with the product strategy and site priorities to drive process and quality improvements, cost reduction, and ensure continuity of supply.

    • US Engineering technical manager for the Aseptic Process Engineering Team in support manufacturing process improvement, capacity scale-up, sustaining engineering and maintenance of business, and strategic programs.
    • Influential leader responsible for technical direction of the team and ownership of the aseptic process technical competency.
    • May manage project portfolios and or individual Sustaining Engineering and/or MOB projects.
    • Interfaces with multiple internal organizations and external suppliers in leading and executing projects and or strategic business initiatives.
    • Provides direction and oversight to Aseptic Process technical team.
    • Supervision of 4 full time employees and 3 contract engineers.

    Responsibilities

    • Leadership of the Aseptic Process Engineering competency and associated resources in the US Pharmaceutical plant including functional management of the group, budget, planning, and projects associated with design, development, technology transfer and production.
    • Develop and execute an engineering strategy for the US pharmaceutical plant based on industry standards and best practices ensuring regulatory compliance through the selection and implementation of the latest technology in facility design, processing equipment and methodologies.
    • Ensure that engineering knowledge, processes and best practices are leveraged across sites and drive manufacturing platform standardization where appropriate.
    • Provide leadership, guidance and support in technology transfers, new product launches, troubleshooting and problem resolution, capital project planning and executions, cost improvement and talent management.
    • Manage a portfolio of Sustaining Engineering Projects aligned with site priorities to drive process and quality improvements, reduce cost, and ensure continuity of supply.
    • Provide oversight and direction to the Pharma Maintenance of Business Portfolio Leader and support MOB projects, activities, and resource plans.

    Key Relationships: 

    • Tampa Manufacturing Site Leadership Team.
    • Tampa site Engineering Director (matrix reporting)
    • Tampa site Procurement and Finance
    • External suppliers, engineering firms, and technical consultants
    • US Engineering Leadership Team including managers and Portfolio Leaders

    Qualifications

    • BS/MS Mechanical Engineering, Chemical Engineering, Materials Science.
    • Experience with facility and equipment start-up and manufacturing in sterile cGMP pharmaceutical operations.
    • Strong background with Sterile GMP guidelines, EU standards.
    • Engineering management and technical staff development.
    • Leadership of large-scale manufacturing improvement programs/projects.
    • Familiarity with FDA regulated products.
    • Project management training or certification.
    • Strong troubleshooting and analytical capabilities with experience in DOE.
    • GMP, Six sigma, DOE, and Design for Manufacturing.
    • Strong communication and interactive skills, capable of leading and directing project teams as required.
    • Understanding Regulatory requirements for ANDA and NDA product and process changes.
    • Product and process development phase/gate methodology and manufacturing tech transfer.
    • Interfacing and communicating with site and corporate leadership.

    Apply here:   www.bauschhealth.com/careers 

  • February 14, 2019 8:38 PM | Anonymous member (Administrator)

    Overview

    Supervise the QC Chemistry Department in agreement with all regulatory requirements. Drive quality improvements of products and processes through active participation in interdepartmental areas. Supervise the QC Chemistry laboratory for in-process, finished product, customer complaint and stability samples for all products manufactured at Bausch + Lomb. Assume the responsibility for the GMP, ISO and Environmental Health and Safety procedure awareness and compliance within the respective areas. Primary back-up for QC Chemistry Lab Manager.

    Responsibilities

    1. Responsible for the supervision and development of all personnel within the QC Chemistry. 
    2. Responsible for the GMP compliance of all functions and processes of the QC Chemistry department and drive continuous improvement.
    3. Back-up role in the transfer of analytical methods and specifications from new products from R&D and CM to QC Chemistry.
    4. Provide analytical testing expertise including oversight and guidance for site engineering, R&D and CM projects and investigations.
    5. Project Management for QC Chemistry departmental projects.
    6. Review, generation and approval of analytical investigations (LIRs) and non-conformances (NCs).
    7. Responsible for the compliance of the supervised individuals to the company training policies for the QC Chemistry Department.
    8. Evaluate and upgrade lab equipment, instruments and software, capacity and efficiency.

    9. Review/approve validation and qualification protocols. Write/review/approve SOPs.

    10. Engage team to identify and implement actions to improve on-time delivery, improve right first time, and improve process efficiency.
    11. Assume the responsibility for the GMP, ISO and Environmental Health and Safety procedure awareness and compliance within the respective area.

    Qualifications

    Education: BS or MS degree in Chemistry / Biology or related scientific discipline.

    Experience: 7-10 years of laboratory work experience of which at least 3-5 years must be in the supervisory role.

    Skills: Must have demonstrated expertise and knowledge of laboratory equipment, Method Development, validation and tech transfer. 

    Other Skills: Must be able to work and solve problems independently as well as part of a team. Able to take on additional duties as required in the team environment. Should have a working knowledge of MS Word and MS Excel.

    Apply Here:  www.bauschhealth.com/careers 

  • February 14, 2019 8:36 PM | Anonymous member (Administrator)


    Overview:

    Shift coordination of Manufacturing activities. Maintain a technical understanding sufficient to provide front-line instruction for production issues.  Assume responsibility for the GMP, environmental health and safety procedure awareness, and compliance within the respective area. Support OpEx initiatives, efficiency, and continuous improvement.

    Duties:

    • Personnel Supervision. Supervise personnel in support of Compounding and Aseptic Prep activities in the pursuit of daily excellence. Assign work to manufacturing personnel. Coordinate the daily workflow with Group Leaders from other shifts.
    • Production Scheduling. Work directly with the Planning Department in development of the production schedule. Identify equipment and personnel requirements and provide solutions for constraints. Coordinate shift activities and facilitate the transfer of activities between shifts. Communicate with internal customers as frequently as required. Coordinate and escalate equipment issues with appropriate technical resources.
    • Personnel Training and Development. Oversees technical training of personnel. Mentors new personnel in behaviors and job expectations. Engages in the identification of training plan based on business needs.  Reports progress to the Team Leader. Participates in development of training plan. Ensures SOP’s are read; provides technical SOP training.
    • Compliance. Understands and enforces daily area compliance in safety/EHS procedures, GMP, and SOP/batch record adherence. Audits area compliance. Evaluates quality performance with the Team Leader and/or Manufacturing Quality Assurance.
    • Operator Substitution. Perform manufacturing compounding and/or aseptic prep operator functions when necessary.
    • Projects. Participate on project teams and R&D projects. Coordinate new product Process Validation and Cleaning Validation activities. Attend GMP training sessions as scheduled.  Represent Manager in project meetings.  Serve as leader of Operational Excellence Projects.  Support OpEx and WISE OWLS initiatives. 
    • Documentation. Review area documentation including batch records and logbooks as necessary.

    Requirements:

    5+ years of sterile pharmaceutical experience. Understanding of compounding, aseptic prep, aseptic filling or packaging including batch preparation, general CIP/SIP, sterilization and cleaning principles.  Proven experience leading people, Multi–tasking, and risk assessments.

    Special Skills:

    Excellent math skills, detail oriented, good communication skills and leadership abilities. Mechanical aptitude to understand principle of operation of various compounding and aseptic prep equipment, self-initiative. Customer service. Ability to work with multiple technical and business disciplines. Understand and apply general chemical, microbiological, and engineering/physics principles. Makes sound business decisions. Must have a general understanding of “why” activities are performed as a daily tool in making sound decisions and troubleshooting problems. Good written and verbal skills. Computer skills (email, word processing, basic spreadsheet). Makes decisions based on data when possible.   

    Apply Here:   www.bauschhealth.com/careers 

  • February 14, 2019 8:31 PM | Anonymous member (Administrator)


    Overview:

    Coordinates the production activities for filling and packaging lines.  Operates filling and packaging equipment.  Receives direction from Team Leader on production plan.  This position requires Aseptic Gowning certification (where applicable), QC certification, ERPLx certification, Visual Inspection certification, and Line Clearance/LOTO certification.  Evaluates quality issues with the QC Team Leader.  Assumes responsibility for the GMP, ISO, environmental health and safety procedure awareness, and compliance within the respective area.  Participates in improvements for material variance, quality indicators, and line efficiencies.  Provides feedback to team leaders regarding associate performance and behaviors.

    Responsibilities:

    1. Assigns tasks for manufacturing operations and support associates. Coordinates and performs the set-up and changeover of manufacturing equipment.  Verifies component readiness, line clearances, and product returns.  Maintains equipment and line cleanliness and compliance (audits).      
    2. Operates filling and packaging equipment for the manufacturing of drug product.
    3. Completes all documentation accurately (review batch records/ERPLx transactions).
    4. Performs initial and ongoing training and development of associates.

    Qualifications:

    Education: HS Diploma/GED required or BA/S preferred.

    Experience: 3 to 7 years in pharmaceutical/FDA regulated facility or related field; experience in leadership positions preferred. Previous filling and packaging manufacturing experience required.  

    Qualifications: Leadership experience preferred.  Basic math skills, detail oriented, excellent communication skills and demonstrated leadership ability.  Ability to effectively work with different department supervisors.   Ability to operate manufacturing equipment.  Strong knowledge of the manufacturing process as well as manufacturing performance and financial attributes such as material variance, yield, and efficiencies.   

    Apply Here:  www.bauschhealth.com/careers

  • February 14, 2019 8:24 PM | Anonymous member (Administrator)


    Job Description

    Responsible for operating manufacturing equipment ensuring target line rates are met. Performs initial troubleshooting and diagnose operational issues. Assist other resources when highly technical issues are addressed.

    Responsibilities:

    1. Responsible for operating manufacturing equipment ensuring target line rates are met. Also responsible to perform line cleaning and clearing, equipment disinfection, predictive maintenance, initial problem assessment for equipment issues, minor adjustments and repairs, load components during run, documentation, provides operational training to other employees. Ensures production areas cleaned and organized to prevent cross – contamination and product related problems. 2. Assist during change over, set up, PMs, major adjustments and repairs, parts design and fabrication, technical training, shutdown planning and projects, generation of work orders and maintenance of spare parts inventory / retrieval and housekeeping of aseptic parts storage area. 3. This position requires Aseptic Gowning certification (where applicable). Assume responsibility for the cGMP, ISO, EHS compliance within the respective area. Uses production metrics to drive process improvements and enhance productivity, QC, Visual Inspection, and Line Clearance/LOTO certification needed. 4. Completes all documentation accurately Support OpEX initiatives.

    Qualifications:

    HS Diploma/GED required or AD preferred Ability to operate manufacturing equipment and perform minor troubleshooting and machine adjustments. Good math and writing skills. Detail orientated with excellent communication skills and quality conscious. Able to work quickly and under pressure.

    Apply Here:  www.bauschhealth.com/careers

  • February 14, 2019 8:16 PM | Anonymous member (Administrator)


    Overview:

    Material Handling - provide components, raw materials, labels (Kits) to manufacturing and bring finished goods and returns to the warehouse.  Handle all waste materials (hazardous and non-hazardous)

    Staging/Prep Material Handling - Prepare components and handle returns for the Core.

    Insert Folding - Run the insert folding machine operation.

    Responsibilities:

    1. Material Handling - Operate pallet jack, motorized pallet jack, sit down forklift, high lift and stretch wrapper. Rocon activities/ trash removal. Tray making. Computer entries (Erplx, PeopleSoft, BPICS).
    2. Scanner use. Delivering kits to the lines. Setting up lines. Deliver finished goods to the warehouse.  Follow cooler procedures. Entries into Filling and Packaging batch records.
    3. Component Breakdown Material Handling - Schedule status and priority setting. Transfer components to CNC area.
    4. Checking release status, Labeling Bags. Proper use of pass through into controlled areas. Cleaning of Staging area. Extra Components to Staging. Processing Returns.
    5. Insert Folding- Run the insert folding operation including cleaning, set up, line clearance, minor maintenance, accountability procedures, and computer entries.

    Qualifications:

    High School Diploma.

    6 hours of GMP/ISO training, Compliance Wire Training, support OpEx and Wise Owl initiatives.

    Specialized Training: Ability to pass FDOH compliance training.

    Pallet Jack, Motorized Pallet Jack, Sit Down Forklift, High Lift Forklift, and Stretch Wrapper.

    Must be able to read, write and speak English and possess basic math skills.

    Apply Here:  www.bauschhealth.com/careers 

  • February 14, 2019 8:13 PM | Anonymous member (Administrator)


    Overview:

    This is a 2nd shift position with possible shift rotation based on business need. 

    Perform routine testing for release of raw materials, and R&D products.  Perform Environmental and Utility Monitoring in aseptic areas.

    Responsibilities:

    • Perform routine assays for endotoxin and bioburden, on various finished products and/or raw materials.
    • Perform testing in conjunction with laboratory investigations.
    • Perform environmental and utility monitoring. Perform testing in support of facility Validation activities.
    • Support OpEx and WISE OWLS initiatives. Read/Record all pertinent data on the appropriate forms or computer system.
    • All other duties as assigned

    Qualifications:

    Ability to work independently with minimal supervision. Experience in computer operation and basis word processing programs. Ability to communicate and work well with others; good oral and written skills. Excellent aseptic technique.  Familiar with microbiological testing techniques concerning product testing.

    Tools and equipment used: Computer, phone, copier, fax, autoclave, scale, dishwasher, cleaning supplies and equipment, media/solution preparation Equipment, lab equipment as necessary.

    High School Diploma or B.S. (Biology, Microbiology or related experience.)

    Must be able to read, write and speak English and possess basic math skills.

    Apply Here:  www.bauschhealth.com/careers 

Bay Area Manufacturers Association | 727-536-5809

P.O. Box 167 | 1324 Seven Springs Blvd. | New Port Richey | Florida | 34655

Powered by Wild Apricot Membership Software