Senior Manager, Operations Support

Posted 12 Days Ago
Be an Early Applicant
Bedford, NH, USA
In-Office
Senior level
Pharmaceutical
The Role
Leads the Operations Support organization across biopharmaceutical manufacturing sites. Responsibilities include managing process specialists, manufacturing and visual inspection schedules, technical documentation, investigations, quality systems, performance metrics, continuous improvement, audit support, client relationships, and team development. The role oversees direct and indirect reports, drives data-informed operational decisions, and supports GMP manufacturing objectives.
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.

   

Essential Duties and Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The essential duties and responsibilities include the following, but other duties may be assigned.

  • 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.

Special Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. The employee must be physically capable to perform the duties listed below with or without reasonable accommodations which may be made to enable individuals with disabilities to perform the essential functions.

  • Ability to stand, sit or remain in the same position for extended periods of time.   
  • May be required to travel between sites at the campus. 
  • Follow written instructions. 
  • Able to train others. 
  • Able to work in a highly complex environment with competing demands and priorities. 

Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  • Primarily interacts with staff in the following departments at all levels: Operations, Quality, Project Management, Engineering, Supply Chain, and MSAT. 
  • Will frequently interact with clients and client representatives.     
  • Will frequently interact with external vendors. 
  • Manage 4-5 Direct reports, supporting a team of 10-15 Indirect Reports. 

TRAVEL – Travel to various PCI locations up to 15% annually.

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 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. 

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 8 years of technical experience in life sciences, biopharmaceutical, biotechnology, or medical device industries with GMP experience
  • Bachelor’s or master’s degree in chemical, mechanical, pharmaceutical engineering, or a related field; comparable education and experience accepted
  • Hands-on experience in process engineering or sciences, manufacturing operations, technical project management, or quality
  • Experience in a biopharmaceutical or medical device manufacturing organization
  • Familiarity with aseptic manufacturing
  • Prior people management or supervisory experience
  • Experience leading large projects and initiatives through completion
  • Strong interpersonal, verbal, and written communication skills
  • Proven leadership, persuasiveness, initiative, and problem-solving abilities
  • Ability to inspire and motivate teams
  • Ability to prioritize and manage multiple resources in a production environment
  • Resilience and adaptability through operational and organizational change

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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