Amneal Pharmaceuticals

Manager, Manufacturing Science & Technology

Amneal Pharmaceuticals$145K — $160K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in a relevant scientific or technical field (e.g., Pharmaceutical Sciences, Chemical Engineering, Microbiology).
  • 5+ years in pharmaceutical manufacturing or technical services.
  • 3+ years specializing in sterile operations, including Blow-Fill-Seal and aseptic fillings.
  • 5+ years in validation lifecycle activities and process characterization.
  • Strong capabilities in technical writing and data analysis.

Responsibilities

  • Provide technical support for various sterile manufacturing processes.
  • Lead validation lifecycle activities and manage tech transfers.
  • Serve as a subject matter expert for deviations and investigations.
  • Establish and improve control strategies for contamination control.
  • Collaborate with cross-functional teams on process improvements and equipment qualifications.
  • Author and review technical documents, supporting audits and regulatory inspections.

Benefits

  • Comprehensive and flexible health and insurance plans.
  • Significant 401(k) matching contribution.
  • Programs promoting employee well-being.
  • Support for work-life balance and personal commitments.
Full Job Description
Job Description

Description:

This role provides technical leadership and hands on support for sterile manufacturing operations, including Blow Fill Seal, prefilled syringe filling, sterile bag filling, formulation, sterile filtration, aseptic processing, component preparation, visual inspection, and related process interfaces. This role ensures sterile processes are scientifically sound, validated, robust, compliant, and continuously improved, serving as a technical bridge between Manufacturing, QA, QC Microbiology, Engineering, Validation, Regulatory Affairs, Supply Chain, and Product Development/Technology Transfer.

Essential Functions:
  • Provide technical support for sterile operations (BFS, prefilled syringes, bag filling, formulation, filtration, aseptic transfers, filling setup, container closure, visual inspection)
  • Lead or support validation lifecycle activities (PPQ, CPV, monitoring, trending) and manage tech transfer, scale up, site transfer, new product introduction, and lifecycle management
  • Serve as MS&T SME for deviations, non conformances, OOTs, failures, yield losses, contamination events; lead investigations, impact assessments, CAPAs, and batch disposition support
  • Establish and improve control strategies (CPPs, CQAs, IPCs, parameters, criteria) and support contamination control, APS, EM trending, cleanroom controls, and sterile assurance investigations
  • Partner with Engineering, Manufacturing, Validation, QA, and Automation on equipment qualification, process improvements, facility upgrades, and manufacturing readiness; lead or support change control assessments
  • Author/review technical documents (protocols, reports, SOPs, risk assessments, CPV, investigations), support audits and regulatory inspections, and provide technical coaching to junior staff and project teams


Qualifications

Education:
  • Bachelors Degree (BA/BS) Pharmaceutical Sciences, Pharmacy, Chemical Engineering, Mechanical Engineering, Biomedical Engineering, Microbiology, Biology, Chemistry, Biotechnology, Life Sciences, or a related scientific or technical field. - Required


Experience:
  • 5 years or more in Experience in pharmaceutical manufacturing, MS&T, technical services, process engineering, validation, process development, sterile operations, or technical operations.
  • 3 years or more in Experience in sterile manufacturing and Blow-Fill-Seal, prefilled syringes, sterile bag filling, sterile filtration, vial filling, cartridge filling, formulation, or aseptic filling
  • 5 years or more in Experience with PPQ, CPV, process characterization, technology transfer, or continued process monitoring.
  • 3 years or more in Experience supporting FDA, EMA, customer, or internal audits, statistical process control, Minitab, JMP, or similar data analysis tools.


Specialized Knowledge:
  • Strong technical judgment in sterile manufacturing and aseptic processing. Ability to troubleshoot complex manufacturing, process, equipment, and contamination-control issues. Strong technical writing, data analysis, and investigation skills. Ability to lead cross-functional teams and influence without direct authority. Strong communication skills with Manufacturing, QA, QC, Engineering, Validation, Regulatory, and Supply Chain. Ability to manage multiple priorities in a fast-paced GMP manufacturing environment. High attention to documentation quality, compliance, audit readiness, and patient safety. Practical, floor-oriented problem-solving mindset with the ability to translate technical knowledge into executable manufacturing solutions.


Additional Requirement: This position requires successful completion of an OSHA-compliant Respirator Fit Test.

The base salary for this position ranges from $145,000 to $160,000 per year. Amneal ranges reflect the Company's good faith estimate of base salary that Amneal reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, geographic location and other relevant skills. At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement. We also promote employee well-being with programs that helps you enjoy your career alongside life's many other commitments and opportunities.

About Amneal Pharmaceuticals

Amneal Pharmaceuticals, Inc. is an integrated specialty pharmaceutical company powered by a robust U.S. generics business and a growing branded business. Together, our team is working to build one of the most dynamic pharmaceutical companies in our rapidly changing industry. Today’s healthcare environment requires a new approach and new ideas. While staying true to our reputation for quality, service and value, we are reinventing our processes, our playbook and our creative partnerships. Our goal is simple: to be a healthy, growing company that endures for decades and that is an indispensable partner to the healthcare providers and patients we serve. Amneal is headquartered in Bridgewater, New Jersey.
Learn more about Amneal Pharmaceuticals
Size
7,000 employees
Market Cap
$616.6 million
Industry
Net Income
$91 million
5 Year Trend
+20.5%
Revenue
$1.9 billion
NASDAQ

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