The Pharma Manufacturing Unit Leader (MUL) is responsible for leading end-to-end manufacturing operations within the Pharma unit, ensuring strict compliance with regulatory standards (FDA, GMP) while ...
The Pharma Manufacturing Unit Leader (MUL) is responsible for leading end-to-end manufacturing operations within the Pharma unit, ensuring strict compliance with regulatory standards (FDA, GMP) while ...
The Pharma Manufacturing Unit Leader (MUL) is responsible for leading end-to-end manufacturing operations within the Pharma unit, ensuring strict compliance with regulatory standards (FDA, GMP) while ...
The Pharma Manufacturing Unit Leader (MUL) is responsible for leading end-to-end manufacturing operations within the Pharma unit, ensuring strict compliance with regulatory standards (FDA, GMP) while ...
Pharma Product Manager- R01564155
New York, NY · On-site +1
$75 - $80/hr
CSPO Job requirements Role: - Pharma Product Manager Location: - Remote JD:-Pharma domain Software ... You will help shape products that improve manufacturing efficiency, support regulatory readiness ...
Pharma Product Manager- R01564155
New York, NY · On-site +1
$75 - $80/hr
CSPO Job requirements Role: - Pharma Product Manager Location: - Remote JD:-Pharma domain Software ... You will help shape products that improve manufacturing efficiency, support regulatory readiness ...
Quality Assurance Inspector / Pharma Manufacturing Duration: 12 months contract, extendable up to 48 months Location: Andover, MA Note: The client has the right-to-hire you as a permanent employee at ...
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Quality Assurance Inspector / Pharma Manufacturing Duration: 12 months contract, extendable up to 48 months Location: Andover, MA Note: The client has the right-to-hire you as a permanent employee at ...
Job Title: Quality Investigation Reviewer / Pharma Manufacturing Duration: 18 months contract, extendable up to 48 months Location: Andover, MA Note: The client has the right-to-hire you as a ...
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Job Title: Quality Investigation Reviewer / Pharma Manufacturing Duration: 18 months contract, extendable up to 48 months Location: Andover, MA Note: The client has the right-to-hire you as a ...
Quality Assurance Inspector / Pharma Manufacturing Duration: 12 months contract, extendable up to 48 months Location: Andover, MA Note: The client has the right-to-hire you as a permanent employee at ...
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Quality Assurance Inspector / Pharma Manufacturing Duration: 12 months contract, extendable up to 48 months Location: Andover, MA Note: The client has the right-to-hire you as a permanent employee at ...
Job Title: Process Development Technician / Pharma Manufacturing Duration: 8 months contract, extendable up to 48 months Location: Andover, MA Note: The client has the right-to-hire you as a ...
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Job Title: Process Development Technician / Pharma Manufacturing Duration: 8 months contract, extendable up to 48 months Location: Andover, MA Note: The client has the right-to-hire you as a ...
Engineering Project Manager / Pharma Manufacturing Duration: 12 months contract, extendable up to 48 months Location: Andover, MA Note: The client has the right-to-hire you as a permanent employee at ...
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Engineering Project Manager / Pharma Manufacturing Duration: 12 months contract, extendable up to 48 months Location: Andover, MA Note: The client has the right-to-hire you as a permanent employee at ...
Quality Assurance Inspector / Pharma Manufacturing Duration: 12 months contract, extendable up to 48 months Location: Andover, MA Hybrid: 3 days in the office and 2 days working from home Note: The ...
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Quality Assurance Inspector / Pharma Manufacturing Duration: 12 months contract, extendable up to 48 months Location: Andover, MA Hybrid: 3 days in the office and 2 days working from home Note: The ...
Equipment Maintenance Technician / Pharma Manufacturing Duration: 11+ months contract, extendable up to 48 months Location: Groton, CT Note: The client has the right-to-hire you as a permanent ...
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Equipment Maintenance Technician / Pharma Manufacturing Duration: 11+ months contract, extendable up to 48 months Location: Groton, CT Note: The client has the right-to-hire you as a permanent ...
Senior Manufacturing Quality Engineer
Lexington, KY · On-site
$88K - $119K/yr
Job Title : Senior Manufacturing Quality Engineer (Pharma) Location: Lexington, KY Duration: Long Term We're looking for a Senior Manufacturing Quality Engineer to support pharma manufacturing ...
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Senior Manufacturing Quality Engineer
Lexington, KY · On-site
$88K - $119K/yr
Job Title : Senior Manufacturing Quality Engineer (Pharma) Location: Lexington, KY Duration: Long Term We're looking for a Senior Manufacturing Quality Engineer to support pharma manufacturing ...
Quality Assurance Technician (Pharma Manufacturing) CANDIDATES MUST BE ABLE TO WORK NIGHT SHIFT 6PM - 6:30AM THEY ALSO MUST BE ABLE TO TRAIN ON DAY SHIFT, THEN THEY WILL MOVE OVER TO NIGHTS ONCE ...
Quality Assurance Technician (Pharma Manufacturing) CANDIDATES MUST BE ABLE TO WORK NIGHT SHIFT 6PM - 6:30AM THEY ALSO MUST BE ABLE TO TRAIN ON DAY SHIFT, THEN THEY WILL MOVE OVER TO NIGHTS ONCE ...
Job Title: HVAC Systems Engineer / Pharma Manufacturing Duration: 7 months contract, extendable up to 48 months Location: Andover, MA Note: The client has the right-to-hire you as a permanent ...
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Job Title: HVAC Systems Engineer / Pharma Manufacturing Duration: 7 months contract, extendable up to 48 months Location: Andover, MA Note: The client has the right-to-hire you as a permanent ...
Data Scientist / Pharma Manufacturing / Remote Work Duration: 12 months contract, extendable up to 24 Months Client Location: Titusville, NJ Note: The client has the right-to-hire you as a permanent ...
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Data Scientist / Pharma Manufacturing / Remote Work Duration: 12 months contract, extendable up to 24 Months Client Location: Titusville, NJ Note: The client has the right-to-hire you as a permanent ...
Senior Associate Manufacturing
Thousand Oaks, CA · On-site
$15.75 - $19/hr
Master's degree OR Bachelor's degree and 6 months of experience in biotech/pharma manufacturing/laboratory or manufacturing support (i.e. laboratories, engineering, facilities, quality) OR Associate ...
Senior Associate Manufacturing
Thousand Oaks, CA · On-site
$15.75 - $19/hr
Master's degree OR Bachelor's degree and 6 months of experience in biotech/pharma manufacturing/laboratory or manufacturing support (i.e. laboratories, engineering, facilities, quality) OR Associate ...
Pharma Manufacturing & Quality Careers (Multiple Openings - cGMP)
Jupiter, FL · On-site
$25 - $29/hr
Pharma Manufacturing & Quality Careers (Multiple Openings - cGMP) Company: PrideStaff on behalf of a Premier Pharmaceutical Contract Manufacturer Location: Northwestern Palm Beach County, FL (Palm ...
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Pharma Manufacturing & Quality Careers (Multiple Openings - cGMP)
Jupiter, FL · On-site
$25 - $29/hr
Pharma Manufacturing & Quality Careers (Multiple Openings - cGMP) Company: PrideStaff on behalf of a Premier Pharmaceutical Contract Manufacturer Location: Northwestern Palm Beach County, FL (Palm ...
Master's degree OR Bachelor's degree and 6 months of experience in biotech/pharma manufacturing/laboratory or manufacturing support (i.e. laboratories, engineering, facilities, quality) OR Associate ...
Master's degree OR Bachelor's degree and 6 months of experience in biotech/pharma manufacturing/laboratory or manufacturing support (i.e. laboratories, engineering, facilities, quality) OR Associate ...
Equipment Calibration Technician / Pharma Manufacturing
Groton, CT · On-site
$22 - $29.75/hr
Equipment Calibration Technician / Pharma Manufacturing Duration: 12 months contract, extendable up to 48 months Location: Groton, CT Note: The client has the right-to-hire you as a permanent ...
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Equipment Calibration Technician / Pharma Manufacturing
Groton, CT · On-site
$22 - $29.75/hr
Equipment Calibration Technician / Pharma Manufacturing Duration: 12 months contract, extendable up to 48 months Location: Groton, CT Note: The client has the right-to-hire you as a permanent ...
Associate Manufacturing
Thousand Oaks, CA · On-site
High school/GED + 2 years biotech/pharma manufacturing/laboratory or manufacturing support (i.e. laboratories, engineering, facilities, quality) work experience OR * Associate's + 6 months biotech ...
Associate Manufacturing
Thousand Oaks, CA · On-site
High school/GED + 2 years biotech/pharma manufacturing/laboratory or manufacturing support (i.e. laboratories, engineering, facilities, quality) work experience OR * Associate's + 6 months biotech ...
Manufacturing Shift Manager - Pharma
Spokane, WA · On-site
$115K - $180K/yr
This role also gets a differential pay add of 10%. Note 2 : 10+ years of Pharma Manufacturing experience in lieu of Bachelor's Degree will also be considered. Job Summary: This Shift Manager will ...
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Manufacturing Shift Manager - Pharma
Spokane, WA · On-site
$115K - $180K/yr
This role also gets a differential pay add of 10%. Note 2 : 10+ years of Pharma Manufacturing experience in lieu of Bachelor's Degree will also be considered. Job Summary: This Shift Manager will ...
Pharma Manufacturing information
See salary details
$12.26 - $14.18
5% of jobs
$14.18 - $16.11
17% of jobs
$16.34 is the 25th percentile. Wages below this are outliers.
$16.11 - $18.03
24% of jobs
The median wage is $18.42 / hr.
$18.03 - $19.95
18% of jobs
$19.95 - $21.88
9% of jobs
$22.22 is the 75th percentile. Wages above this are outliers.
$21.88 - $23.80
7% of jobs
$23.80 - $25.72
3% of jobs
$25.72 - $27.64
3% of jobs
$27.64 - $29.57
3% of jobs
$29.57 - $31.49
5% of jobs
$31.49 - $33.41
4% of jobs
$12
$20
$33
How much do pharma manufacturing jobs pay per hour?
What are the key skills and qualifications needed to thrive in Pharma Manufacturing, and why are they important?
What is the difference between Pharma Manufacturing vs Pharmaceutical Quality Control?
| Aspect | Pharma Manufacturing | Pharmaceutical Quality Control |
|---|---|---|
| Primary Focus | Production of medicines and active pharmaceutical ingredients | Inspection and testing of products to ensure quality standards |
| Work Environment | Manufacturing plants, production lines | Laboratories, quality assurance labs |
| Required Certifications | GMP training, technical certifications | GMP, quality assurance certifications |
| Industry Usage | Used by pharmaceutical manufacturers during production | Used by quality control teams to verify product quality |
Pharma Manufacturing involves the actual production of medicines, focusing on manufacturing processes and compliance. Pharmaceutical Quality Control centers on testing and inspecting products to ensure they meet safety and quality standards. Both roles are essential in the pharmaceutical industry but serve different functions within the drug development and production process.
How to get a job in pharmaceutical manufacturing?
What is pharmaceutical manufacturing?
What jobs are there in the pharmaceutical industry?
What is pharma manufacturing?
What are some common challenges faced in a Pharma Manufacturing role, and how are they typically addressed?
What is the highest paying job in pharmaceuticals?

Full-time
Posted 23 hours ago
BD rating
7.3
Based on 139 frontline employees who took The Breakroom Quiz
269th of 433 rated machine equipment manufacturers
Job description
BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.
Job Description
The Pharma Manufacturing Unit Leader (MUL) is responsible for leading end-to-end manufacturing operations within the Pharma unit, ensuring strict compliance with regulatory standards (FDA, GMP) while driving operational excellence and delivering business performance targets. This role oversees cross-functional teams to ensure safe, high-quality, and efficient production, aligned with BD's transformation, compliance remediation, and continuous improvement initiatives.
As a Pharma Manufacturing Leader, this position operates in a highly controlled environment involving chemical and biological products, where risk is directly associated with dose accuracy, product potency, and contamination control. The role places a critical emphasis on robust process control, sterility assurance, and reproducibility to guarantee consistent product quality and patient safety.
Job Responsibilities:
Operational Leadership
- Lead end-to-end daily manufacturing operations for the Pharma unit, ensuring strict adherence to production plans, safety protocols, and quality standards.
- Provide clear and consistent direction to frontline leaders and production teams across all shifts to ensure alignment and execution discipline.
- Drive effective implementation of Tiered Management and Daily Management Systems (TMS) to establish clear priorities and maintain operational control.
- Oversee core pharma operations, including formulation, aseptic processing, and filling activities.
- Maintain daily focus on:
- Deviations and batch disposition
- Environmental monitoring and cleanroom compliance
- Sterility assurance and contamination control
- Operate with a low tolerance for process variation, ensuring consistency and reproducibility.
- Manage changes through a highly structured change control process, recognizing that:
Every change carries potential regulatory and validation impact (changes may require re-validation, requalification, or regulatory approval). - Ensure strict adherence to:
- Batch record review and documentation practices
- QC testing and formal release processes
- Oversee operations within highly controlled environments, including:
- Cleanroom classifications (Grades A-D)
- Environmental and contamination controls
- Gowning, airlocks, and facility compliance standards
- Recognize that facilities and utilities are integral to process validation and product quality.
Compliance & Quality
- Ensure full compliance with FDA regulations, GMP standards, BD Quality Systems, and internal procedures, maintaining an always audit-ready environment.
- Lead inspection readiness and actively support regulatory audits (FDA, internal, and external).
- Drive timely and effective resolution of deviations, non-conformances (NCRs), and audit findings through robust CAPA processes.
- Reinforce a strong quality culture with accountability at all levels, grounded in the principle:
"Follow the process exactly and prove every batch meets specification." - Maintain focus on critical pharma risks including dose accuracy, potency, and contamination control.
People Leadership & Engagement
- Lead, coach, and develop supervisors and production teams to build a high-performing, compliant, and accountable organization.
- Ensure adequate staffing, capability building, and succession planning for business-critical roles.
- Demonstrate discipline, rigor, and a zero-tolerance mindset for deviations.
- Foster a culture of strong governance, documentation excellence, and audit readiness.
- Balance operational performance with compliance priorities by:
- Driving compliance discipline and deviation reduction
- Accepting structured, deliberate decision-making processes
- Maintaining focus on contamination control, batch release, and inspection readiness.
- Promote BD Values, a strong Speak Up culture, and an inclusive, respectful work environment.
Operational Excellence & Continuous Improvement
- Lead Lean and BD Excellence initiatives, including Kaizen events, process standardization, and waste elimination.
- Deliver productivity improvements and cost targets aligned with the Cost-to-Win (CTW) strategy.
- Leverage KPIs and data analytics to drive performance, with particular focus on deviation reduction, batch release efficiency, and right-first-time execution.
- Support Factory Blueprint implementation and sustain standard work practices across the unit
Safety & EHS
- Ensure compliance with EHS standards and promote a zero-incident safety culture.
- Address risks proactively and lead investigations for safety incidents.
- Partner with EHS to drive preventive actions and regulatory compliance.
Cross-functional Collaboration
- Partner with Quality, Engineering, Maintenance, Supply Chain, and HR to ensure seamless and compliant operations.
- Support new product introductions (NPI), validation activities, and process transfers.
- Align resources to meet production and business priorities.
BD Excellence, TMS, and Continuous Improvement
- Lead the TMS cycle and set the 24-hour direction for the Manufacturing Unit.
- Sustain BD Excellence through Daily Tier Meetings (DTM), Clean/Inspect/Lubricate (CIL/CL) standards, and loss elimination practices.
- Drive short- and long-term improvements aligned with SQDCP (Safety, Quality, Delivery, Cost, People) objectives.
Other Responsibilities
- Perform additional duties as required to support the needs of the business and site operations.
Education and Experience:
- Bachelor's Degree in Engineering, Life Sciences, Manufacturing, or related field required. Master's Degree preferred
- 5+ years of manufacturing experience in Pharma is required.
- Minimum 3-5 years in people leadership roles
- Strong experience with FDA regulations, GMP compliance, and audit management
- Proven track record in continuous improvement (Lean, Six Sigma preferred)
- Flexibility to support multiple shifts and business needs
- Ability to work in a fast-paced, highly regulated manufacturing environment.
Knowledge and Skills:
- Strong knowledge of pharmaceutical/medical device manufacturing processes
- Experience with deviation management, CAPA, and quality systems
- Familiar with ERP systems (e.g., SAP, Workday) and production planning tools
- Data-driven mindset with ability to analyze and act on performance metrics
- Strategic thinking and execution
- Strong decision-making and problem-solving skills
- Effective communication across all organizational levels
- Change management and transformation leadership
- Collaboration and influence across cross-functional teams
Work Environment:
On-site role in a clean, highly regulated, high-volume medical device/pharma manufacturing facility. Requires interaction with Quality, Production, EHS, Engineering, and Facilities teams.
Why Join Us?
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you'll discover a culture in which you can learn, grow and thrive.
We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.
To learn more about BD visit https://bd.com/careers.
Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.
Required Skills
Optional Skills
Primary Work Location
USA TX - El Paso - Northwestern Dr.
Additional Locations
Work Shift
About BD
Sourced by ZipRecruiter
BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues.
Industry
Medical equipment and supplies manufacturing and manufacturing
Company size
10,000+ Employees
Headquarters location
Franklin Lakes, NJ, US