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Pharma Manufacturing Jobs (NOW HIRING)

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 ...

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 ...

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 ...

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 ...

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Pharma Manufacturing information

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How much do pharma manufacturing jobs pay per hour?

As of Jul 23, 2026, the average hourly pay for pharma manufacturing in the United States is $20.84, according to ZipRecruiter salary data. Most workers in this role earn between $16.35 and $23.32 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in Pharma Manufacturing, and why are they important?

To thrive in Pharma Manufacturing, you need a solid background in life sciences or engineering, strong knowledge of Good Manufacturing Practices (GMP), and relevant industry experience. Familiarity with manufacturing equipment, process automation systems, and regulatory compliance certifications (such as GMP or ISO) is typically required. Attention to detail, problem-solving abilities, and effective teamwork are crucial soft skills in this field. These competencies ensure consistent product quality, regulatory compliance, and efficient production processes essential for patient safety and company success.

What is the difference between Pharma Manufacturing vs Pharmaceutical Quality Control?

AspectPharma ManufacturingPharmaceutical Quality Control
Primary FocusProduction of medicines and active pharmaceutical ingredientsInspection and testing of products to ensure quality standards
Work EnvironmentManufacturing plants, production linesLaboratories, quality assurance labs
Required CertificationsGMP training, technical certificationsGMP, quality assurance certifications
Industry UsageUsed by pharmaceutical manufacturers during productionUsed 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?

To get a job in pharmaceutical manufacturing, candidates typically need a high school diploma or equivalent, with many roles requiring a bachelor's degree in pharmacy, chemistry, or a related field. Relevant skills include knowledge of Good Manufacturing Practices (GMP), attention to detail, and familiarity with manufacturing equipment; certifications such as cGMP training can enhance prospects. Entry-level positions often require on-the-job training, and experience in a regulated environment is valued by employers.

What is pharmaceutical manufacturing?

Pharmaceutical manufacturing involves producing medications and vaccines in controlled environments using specialized equipment and processes. It requires adherence to strict quality standards, Good Manufacturing Practices (GMP), and often involves tasks such as formulation, filling, packaging, and quality testing. Workers in this field need attention to detail, technical skills, and knowledge of safety regulations.

What jobs are there in the pharmaceutical industry?

Jobs in the pharmaceutical industry include roles such as pharmaceutical manufacturing technician, quality control analyst, research scientist, regulatory affairs specialist, production supervisor, and validation engineer. These positions often require knowledge of Good Manufacturing Practices (GMP), laboratory skills, and relevant certifications or degrees. The industry offers opportunities in research, production, quality assurance, and regulatory compliance environments.

What is pharma manufacturing?

Pharma manufacturing refers to the process of producing pharmaceutical drugs on a large scale. This involves the formulation, production, testing, packaging, and quality assurance of medications to ensure they meet regulatory standards. The industry follows strict guidelines to maintain product safety, efficacy, and consistency. Pharma manufacturing can include both the creation of active pharmaceutical ingredients (APIs) and the final dosage forms like tablets, capsules, or injectables.

What are some common challenges faced in a Pharma Manufacturing role, and how are they typically addressed?

One of the most common challenges in pharma manufacturing is maintaining strict compliance with regulatory standards while ensuring product quality and consistency. Employees must adhere to Good Manufacturing Practices (GMP) and undergo regular audits, which can be demanding but also offer valuable learning experiences. Additionally, adapting to new technologies and process changes is essential, as the industry is constantly evolving. Strong teamwork and clear communication with quality assurance, engineering, and R&D departments help address these challenges and maintain smooth operations.

What is the highest paying job in pharmaceuticals?

In pharmaceutical manufacturing, senior executive roles such as Vice President of Manufacturing or Director of Operations tend to be the highest paying positions, often earning six-figure salaries. These roles require extensive industry experience, leadership skills, and knowledge of regulatory compliance and production processes.
More about Pharma Manufacturing jobs
What cities are hiring for Pharma Manufacturing jobs? Cities with the most Pharma Manufacturing job openings:
What states have the most Pharma Manufacturing jobs? States with the most job openings for Pharma Manufacturing jobs include:
Infographic showing various Pharma Manufacturing job openings in the United States as of July 2026, with employment types broken down into 90% Full Time, 4% Part Time, 1% Temporary, 3% Contract, and 2% Nights. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $43,341 per year, or $20.8 per hour.
Manufacturing Unit Leader- Pharma

Manufacturing Unit Leader- Pharma

Becton, Dickinson and Company

El Paso, TX • On-site

Full-time

Posted 23 hours ago


BD rating

7.3

Company rating: 7.3 out of 10

Based on 139 frontline employees who took The Breakroom Quiz

269th of 433 rated machine equipment manufacturers


Job description

We are the people who give possibilities purpose
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
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Primary Work Location
USA TX - El Paso - Northwestern Dr.
Additional Locations
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About BD

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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

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