QA Specialist II - Doc Control

PCI TRGR Penn Pharmaceutical Services Ltd; Bedford (NH); In loco; USD 70.000 - 95.000; Tempo pieno

Descrizione del lavoro

PCI Pharma Services in Bedford, NH seeks a QA Specialist II – Document Control to manage cGMP documentation, master documents, and records. You will coordinate document workflows, prepare batch records, and support audits to ensure compliant release of controlled documents.

The role requires a high school diploma with extensive document control experience in biotech/pharma and strong communication, organizational, and problem-solving skills.

Competenze

• High School Diploma and 10+ years in industry with 6+ years in document control in biotech/pharma/medical device.
• Strong written and verbal communication across levels.
• Experience with cGMPs, FDA/EU requirements is preferred.

Mansioni

• Maintain Quality System Master Documents and Master Document List.
• Facilitate workflows in electronic document management systems.
• Create, modify and approve client batch records.
• Issue and reconcile batch records, lab books, and quality system documents.
• Lead audit preparation and support audit requests.
• Train others in document control processes and develop new tools.

Conoscenze

Communication skills

Attention to detail

Organizational skills

Decision making

Project leadership

Formazione

High School Diploma

Strumenti

MS Office

eQMS systems

Descrizione del lavoro

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.

Position Title: QA Specialist II - Document Control

Location: Bedford, New Hampshire

Department: Quality Assurance, Document Control

Reporting To: Supervisor, Document Control

Responsible For (Staff): No

The individual will manage, coordinate, and maintain cGMP documentation, procedures, and records to ensure only controlled copies are reviewed, approved, issued, distributed, and archived. The Document Control QA Specialist II will evaluate document needs and participate in the processing of Documents and Records, maintain databases and Quality Management System tools and supports personnel and functional areas as needed. The primary objective of the Document Control QA Specialist II will be to contribute to the maintenance and improvement of the Document Control program and its systems. The QA Doc Control group is dedicated to the continuous improvement of the Document Change Control Lifecycle and Quality Systems to meet current compliance standards and ensure proper processing and release of controlled documents.

ESSENTIAL DUTIES AND RESPONSIBILITIES

• Maintain Quality System Master Documents and Master Document List
• Facilitates workflows in the electronic document management system and legacy paper processes.
• Performs the creation, modification, and approval of Client Batch Records independently.
• Issues and reconciles batch records, testing data capture sheets, lab books, equipment log books, room log books, and Quality System event documents.
• Maintains Document, Material and Batch numbering logs.
• Writes and develops QA SOPs with minimal oversight.
• Administers the maintenance of the Record/Document filing system at designated sites.
• Proofs and edits document changes including minor SOP updates, as directed.
• Participate in or lead audit preparation and reconciliation.
• Support audit requests.
• Perform internal audit tasks.
• Supports metrics / report generation.
• Cross-trains and provides support for coverage of multiple production facilities as needed.
• Covers absences.
• Lead continuous improvement efforts and projects across the department, or multiple departments.
• Provide input, propose resolutions.
• Performs obsolete and administrative document workflow within Master Control.
• Leads Quality System Investigation and CAPA action items
• Train others in doc control processes.
• Develops and implements new tools and processes for Document Control with minimal oversight.
• Participate in or facilitate functional area programs.

QUALIFICATIONS

Required

• High School Diploma; and at least 10 years of industry experience with a minimum of 6 years document control experience in the Biotech, Pharmaceutical or Medical Device industries is required.
• Previous Document Control and/or eQMS configuration and system management experience required.
• Advanced knowledge of cGMPs, EU regulatory requirements, and FDA 21 CFR Parts 210,211 and 820 and Industry best practices required.
• Working knowledge of Computer System Validation and Change Control requirements.
• Assist is leading large or cross-functional projects and improvement initiatives as assigned.

Preferred

• Superior professional communication skills across all levels of the organization written and verbally Superior customer service.
• Identify and lead large or cross-functional projects and improvement initiatives.
• May support more than one production facility.
• Expert skill level in MS Office, general computer uses and the electronic Quality Management System and associated tools.
• Excellent professional written and verbal skills.
• Team oriented.
• Excellent Organizational skills.
• Highly Efficient.
• Excellent attention to detail.
• Perform repetitive tasks with high level of detail, requiring decision making on daily tasks and improvement initiatives.
• Sound decision making ability required.
• Recommend solutions to Management for critical decisions.

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.

Why work for PCI Pharma Services?

At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience.

Our people make all of this happen, so providing an industry leading experience for our people is equally as important.

By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers.

We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program.

We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don't say no, we figure out how.