Supervisor, Manufacturing, M-F 4PM to 12:30 AM

Posted 3 Days Ago
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Bedford, NH, USA
In-Office
Senior level
Pharmaceutical
The Role
Lead a 12-hour aseptic manufacturing shift ensuring cGMP/FDA compliance. Supervise staff to execute equipment preparation, compounding, filtration, isolator filling, and lyophilization. Manage schedules, training, KPIs, investigations, deviations and CAPAs; drive safety, inspection readiness, process improvement, and cross-functional coordination.
Summary Generated by Built In

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.


We are PCI. 


Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.

   

The Manufacturing Supervisor leads a manufacturing team in a variety of complex tasks in accordance with the FDA and other regulatory agencies while following all safety guidelines of PCI. They will be responsible for supervising a 12-hour production shift for aseptic manufacturing including equipment preparation, formulation, filtration, aseptic / non-aseptic compounding, filling in an isolator and Lyophilization activities. Ensure execution of production plan across multiple shifts and manage staff performance against department’s operational goals.

  • Ensure safety of manufacturing area and work practices in accordance with all PCI Health, Safety and Environmental program.

  • Be highly visible, hands-on team builder to motivate, coach, support, inspire and retain highly effective teams while managing for high performance and developing others

  • Coordinate and supervise Manufacturing personnel in the cGMP operations to meet all scheduled manufacturing work

  • Guide and train employees to ensure FDA and other regulatory agency requirements have been properly implemented and are continually met.

  • Plan and execute manufacturing instructions in order to perform equipment preparation, compounding, filtration, formulation and fill activities for aseptic and terminally non aseptic products in accordance with Good Manufacturing Practices (GMP)

  • Provide leadership, guidance, and direction to staff in alignment with cGMP requirements, department goals and corporate quality standards

  • Partner with Planning to ensure effective prioritization and schedule adherence and to meet all required capacity demands

  • Collaborate with enabling groups to optimize processes

  • Recruit and supervise staff to execute department functions; ensure effective utilization of resources through consistent performance management

  • Proactively identifies, assesses, and mitigates operational and organizational risks; escalate key risks and issues to manufacturing senior management and cross-functional support teams

  • Establish key performance indicators in alignment with department goals, maintain and report applicable area or organizational metrics

  • Collaborate with training to design department training plan and training plan execution. Ensure Training materials are accurate and sufficiently detailed

  • Commit and work to honor timely completion of investigations and deviations and CAPAs. Utilize quality metrics to measure, analyze, and improve team performance. Ensure Real time batch review and "Right First Time"

  • Enhance and reinforce Inspection readiness of assigned manufacturing areas. Participates in inspections conducted by external regulators 

  • Identifies continuous improvement opportunities to improve processes and practices

Qualifications: The requirements listed below are representative of the knowledge, skill, and/or ability required for the stated position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  • Minimum High School Diploma

  • 5-7 years of experience in a GMPs environment required

  • 3-5 years of experience leading direct reports or teams is preferred

  • Experience with GMPs, FDA and other regulated agency environments is required

  • Experienced in making real time decisions on safety, process, scheduling and personnel-related issues.

  • Ability to prioritize and manage multiple resources in a production environment with flexibility to meet organizational needs

  • Proven leadership, persuasiveness, initiative, and problem solving skills

#LI-LL1

Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future

Equal Employment Opportunity (EEO) Statement:
PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of 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, or any other protected status.

At PCI, Equity and Inclusion are at the core of our company’s purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity – at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

Skills Required

  • Minimum High School Diploma
  • 5-7 years of experience in a GMP environment
  • Experience with GMPs, FDA and other regulated agency environments
  • Experienced in making real time decisions on safety, process, scheduling and personnel-related issues
  • Ability to prioritize and manage multiple resources in a production environment
  • Proven leadership, initiative, persuasiveness, and problem solving skills
  • 3-5 years of experience leading direct reports or teams

PCI Pharma Services Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about PCI Pharma Services and has not been reviewed or approved by PCI Pharma Services.

  • Retirement Support Feedback suggests the company provides a 401(k) with an employer match in the mid‑single‑digit range, with immediate vesting noted in certain cases. This is viewed as a solid component of the overall package.
  • Leave & Time Off Breadth PTO and paid holidays are commonly available, and some roles indicate vacation is accessible from early tenure. Availability of time off is frequently described as a positive element of the package.
  • Affordable Benefits Health insurance is sometimes described as reasonably priced depending on plan tier. Feedback suggests core medical, dental, and vision coverage is part of a standard offering.

PCI Pharma Services Insights

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The Company
HQ: Philadelphia, PA
2,259 Employees

What We Do

PCI is a leading provider of integrated pharmaceutical development services to the global healthcare market. With facilities in North America and Europe, PCI supports pharmaceutical and biotech companies with products destined for more than 100 countries around the world. PCI provides services for each stage of the product lifecycle – from early Phase I through commercial launch and long-term supply – and partners with customers to provide key insight and expertise in enabling successful commercialization and bringing lifesaving medications to patients. For more information, go to www.pci.com.

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