Quality Manager, NPI

Posted 2 Days Ago
Be an Early Applicant
Hiring Remotely in Rockford, IL, USA
In-Office or Remote
87K-98K Annually
Expert/Leader
Pharmaceutical
The Role
Lead a team managing Design Control and Quality Assurance for New Product Introduction (NPI) of combination products. Develop and implement QA strategies, manage project timelines and risks, ensure regulatory compliance, drive change control and CAPA, collaborate with stakeholders and customers, support audits and inspections, and represent NPI quality in cross-functional, multi-site teams.
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 are the following but other duties may be assigned.  

  • Lead a team of Quality Professionals responsible for managing Design Control activities for NPI projects and direct cross-functional team members to achieve on-time quality deliverables, pristine customer service, value-add results.
  • Ensures delivery of all quality elements needed to facilitate new product introductions of combination products.
  • Develop Advanced Drug Delivery Product Quality Assurance strategies and implements agreed strategy to support the development of NPI projects.
  • Makes key decisions on product quality, compliance, and regulatory conformance issues for combination products and ensures risk-based escalations to leadership.
  • Working with the programme and project managers manage project timelines to ensure Quality elements of projects are delivered on time and critical paths are identified and monitored throughout their lifecycle.
  • Promote engagement at all levels and stages of the program. Encourage individuals to contribute to the success of each project and illustrate benefits brought about.
  • Manage risks within the program - ensuring risks are identified, evaluated, and controlled through the program lifecycle.
  • Follow and comply with the NPI process as per company procedures and policies.
  • Display strong leadership to the various project teams from concept to handover. Lead by example in day-to-day project and team management.
  • Manage change at varying levels ensuring site procedures are followed and change controls are raised at the appropriate time with the relevant approvers engaged from the outset.
  • Create and sustain a working environment that promotes the PCI Values and Behaviours.
  • Collaborate with Customer to define KPI’s and lead reporting of KPI’s to Site and Customer Teams
  • Manage and ensure the quality element of all new products/devices and their associated project phases. It is a requirement of this role that on occasion the individual will be required to travel on company business. This may be vendor/supplier or customer based.
  • Maintain, continually improve, and ensure a compliant NPI Change Requests that promotes sound technical review of product development changes, design reviews, impact assessments, relevant documentation, and compliant closure.
  • Serve as a an NPI risk management representative on cross-functional and multi-site teams to support integrating risk management into various product quality systems such as Change Control and CAPA.
  • Collaborate with internal stakeholders and clients in providing feedback on issue management, escalation, evaluation, and resolution for quality, operational, and regulatory concerns.
  • Participate in, present on, and/or provide rationale for the NPI program during periodic audits and regulatory inspection and customer visits/conference calls as required.
  • This position may require overtime and/or weekend work.
  • Performs other duties as assigned by Director.

                                                                                                         

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

  • Stationary Position: From 1/2 to 3/4 of the day.  
  • Move, Traverse: Up to 1/4 of the day.
  • Operate, activate, use, prepare, inspect, or place: Up to 1/4 of the day.  
  • Install, place, adjust, apply, measure, use, or signal: None.  
  • Ascend/Descend or Work Atop: None.
  • Position self (to) or Move (about or to): None.
  • Communicate or exchange information: 3/4 of the day and up.
  • Detect, distinguish, or determine: Up to 1/4 of the day.  

On an average day, the individual can expect to move and/or transport up to 10 pounds less than 1/4 of the day. 

This position may have the following special vision requirements.

☒ Close Vision ☒ Distance Vision ☒ Color Vision ☒ Peripheral Vision ☒ Depth Perception ☒ Ability to focus ☐ No Special Vision Requirements    

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

The following are some environmental conditions that one may be exposed to daily and for various lengths of time. 

Ø Work is primarily performed at a desk and/or in an office environment. for 1/2 to 3/4 of the day.  Ø The noise level in the work environment is typically quiet. 

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

Required:

  • Bachelor’s degree in engineering, Life Sciences, or related technical discipline.
  • Minimum of 10+ years of progressive experience within pharmaceutical, biotech, or medical device industries. Expert knowledge of GAMP 5, 21 CFR Parts 820, 210/211, and 11, and data integrity regulations.
  • Strong understanding of Product Life Cycle Management, Design Assurance, and Project Management.
  • Full Professional Proficiency: Ability to speak, read, and write fluently and accurately on all levels pertinent to professional needs.
  • Strong quality assurance/control, manufacturing, laboratory, technical support, regulatory, and/or validation background is required
  • Highest Reasoning Ability: Ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems and deal with nonverbal symbolism in its most difficult phases while dealing with concrete/abstract variables.
  • High Standard of Report Writing
  • Ability to effectively present information to various people as the job requires. 
  • Ability to identify and resolve problems in a timely manner. 
  • Ability to display original thinking and creativity.  
  • Ability to show success in managing employees.  
  • Ability to demonstrate attention to detail. 
  • Ability to set and achieve challenging goals.                  

The hiring rate for this position is $86,880-$97,740 plus eligibility for an annual 10% performance bonus. Final offer amounts are determined by multiple factors, including but not limited to specific and relevant experience, education, credentials, geography, and subject matter expertise. PCI offers full-time employees a competitive benefits package that includes paid time off, health insurance coverage (including dental and vision), a flexible spending account, and a 401(k) plan.

#LI-SW1

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

  • Bachelor's degree in engineering, Life Sciences, or related technical discipline.
  • Minimum of 10+ years progressive experience within pharmaceutical, biotech, or medical device industries.
  • Expert knowledge of GAMP 5, 21 CFR Parts 820, 210/211, and 11, and data integrity regulations.
  • Strong understanding of Product Life Cycle Management, Design Assurance, and Project Management.
  • Strong quality assurance/control, manufacturing, laboratory, technical support, regulatory, and/or validation background.
  • Full professional proficiency in speaking, reading, and writing English.
  • Demonstrated success managing employees and providing leadership to project teams.
  • High-level report writing, presentation, problem-solving, attention to detail, and ability to set and achieve challenging goals.
  • Ability to follow NPI processes, manage change controls, and integrate risk management into quality systems (Change Control, CAPA).

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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