Sr Manager, Operations

Posted Yesterday
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Bedford, NH, USA
In-Office
Senior level
Pharmaceutical
The Role
Lead Operations Support across multiple Bedford manufacturing sites, overseeing technical writing, investigations, finite scheduling, project management, GMP compliance, metrics, continuous improvement, audits, customer interfacing, and team development. Travel up to 15% annually.
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.

   

Summary of Objective:

The Senior Manager of Operations Support reports directly to the Senior Director of Operations and is responsible for overseeing technical writing, investigations, finite scheduling, and project management across multiple PCI manufacturing sites within the Bedford campus. This role serves as a key leader on the Operations Leadership Team.  The role is critical to ensure ongoing GMP compliance and adherence to quality standards across all department staff and processes.

Essential Duties and Responsibilities:

  • Provide technical leadership and strategic oversight for the Operations Support group across multiple PCI Manufacturing sites at the Bedford campus.

  • Build and lead a team of process specialists who will work closely together and within a highly matrixed, cross-functional team to successfully deliver business objectives.

  • Develop and manage Manufacturing and Visual Inspection (VI) finite schedules to align with customer demands and PCI objectives.

  • Plan and prioritize technical writing projects, including: investigations, Quality Systems (Change Controls, CAPAs, etc.), Standard Operating Procedures (SOPs), and other documentation, in collaboration with cross-functional teams.

  • Lead a team that oversees investigations to drive resolution of deviations, ensuring effective root cause analysis and corrective actions.

  • Establish, analyze, and maintain key performance metrics, including: safety, quality, on-time/right-first-time delivery, inventory, and productivity. 

  • Develop and implement strategies for continuous improvement across manufacturing processes that reduce cost, save time, improve process attributes, and optimize quality.

  • Interpret manufacturing process data, identify trends, troubleshoot problems, and drive data-driven decision-making with effective and concise communications.

  • Serve as a department Subject Matter Expert (SME) during customer and regulatory audits.

  • Interface directly with all clients to ensure the highest level of customer satisfaction is achieved.

  • Act as a highly visible, hands-on leader, responsible for coaching, mentoring, and developing high-performing teams while fostering a culture of accountability and excellence.

  • Oversee the professional development of the Operations Support team, conducting individual performance reviews, setting goals, and driving employee growth.

  • Travel to various PCI locations up to 15% annually.

Qualifications:

  • Minimum of 8 years of technical experience with Life Sciences (Biopharmaceutical / Biotechnology) and/or Medical Device with GMP industry experience.

  • BS/MS in chemical, mechanical, pharmaceutical engineering or relevant work experience.  Comparable blends of education and experience is acceptable.   

  • Strong hands-on experience in either Process Engineering/Sciences, Manufacturing Operations, Technical Project Management, and or Quality.  Experience preferably in a biopharmaceutical or medical device manufacturing organization with familiarity with aseptic manufacturing a plus.

  • Prior people managing experience, supervisory experience at a minimum.

  • Experience leading and driving large projects and initiatives to completion.

  • Positive attitude with strong interpersonal skills. 

  • Proven leadership, persuasiveness, initiative, and problem-solving abilities. 

  • Strong communication skills, both verbal and written. 

  • Able to inspire and motivate. 

  • Self-motivated with a drive for excellence. 

  • Resilient through operational and organizational change. 

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

#LI-AK2

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 of 8 years technical experience in biopharmaceutical/biotechnology or medical device manufacturing with GMP
  • BS/MS in chemical, mechanical, or pharmaceutical engineering or equivalent blend of education and experience
  • Hands-on experience in Process Engineering/Sciences, Manufacturing Operations, Technical Project Management, or Quality
  • Prior people management or supervisory experience
  • Experience leading and driving large projects and initiatives to completion
  • Experience with technical writing, investigations, change controls, CAPAs, and SOPs
  • Ability to serve as SME during customer and regulatory audits (GMP/regulatory audits)
  • Strong communication, leadership, coaching, mentoring, and problem-solving skills
  • Willingness to travel to various PCI locations up to 15% annually
  • Familiarity with aseptic manufacturing

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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