Document Control Specialist at WEST PHARMACEUTICAL SERVICES SINGAPORE PTE LTD

Loyalsock Township, Pennsylvania, United States -

Full Time

Start Date

Immediate

Expiry Date

18 Jul, 26

Salary

0.0

Posted On

19 Apr, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Document control, Quality systems, Good manufacturing practices, GMP, MasterControl, SAP, SharePoint, Batch review, Regulatory compliance, Auditing, Data entry, Technical writing, Problem solving, Communication skills, Microsoft Office Suite, Lean Sigma

Industry

Pharmaceutical Manufacturing

Description

At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future? There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families. We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts. This is an onsite position requiring the team member to be onsite 5 days a week. No relocation is provided for this opportunity. The hours for this role are M-F 7:30AM-4:00PM. Job Summary In this role, you will support the document system to ensure documentation and record keeping processes conform to regulatory requirements as well as internally approved procedures, Distribute documentation necessary to perform cGMP activities and maintain customer documentation, and Manage the final batch review and release process. This role will also be responsible for executing transactions in relevant GMP systems (MasterControl, SAP, Share Point) and other quality functions as applicable including site audit support.Essential Duties and Responsibilities Assist in managing and maintaining traceable, accountable, password protected, documentation system in compliance with site and corporate guidelines to handle the needs of the facility for WKIs, SOPs, ESOPs, validations, training, and other various documentation. Provide instruction on documentation structures and format to ensure compliance to procedures, relevant regulations and standards. Performs document control functions, including document review, editing, tracking, processing, approval, distributing, issuance and archiving in compliance to internal and external requirements. Provides a “Customer Service” attitude when interacting with internal and external customers while accomplishing work, production, and achieving quality standards. Assist in maintaining electronic document control system to ensure prompt retrieval of documents. Review documentation for accuracy and conformance to established guidelines, policies, and practices. Conducts periodic reviews of all documents to maintain consistency alignment to customer, corporate, regulatory, or standard requirements. Write or assist with the development of procedures and work instructions. Serve as System Sub-administrator of the document management system. Makes periodic clean-out of records and samples exceeding minimum retention requirements as per West procedures. Manage the final batch review and release process to ensure all batches meet defined specifications, GDP, ALCOA++, etc. Provide batch release documentation (COC/COA documents) to internal and external customers. Perform data entry tasks in support of Quality System data analysis activities/ KPIs. Provide support with the internal/external audits to include monitoring audit findings. Audit facilities/departments for compliance to the documented QMS and cGMP requirements. Contributes to continuous process improvement efforts. Other duties as assigned. Education Preferred: Associate degree in technical or business-related field. Work Experience Preferred: 3-5 years’ work experience in regulated Quality Control and/or Medical Device or Pharmaceutical Manufacturing Environment. 3+ years Document Control management activities Relevant work history and/or experience may be considered in lieu of degree required and Experience with managing Document Control activities within a regulated industry required and Experience with quality systems such as ISO 9001, ISO 13485, 21 CFR 820 preferred and Experience with MasterControl (preferred) or electronic document management systems Preferred Knowledge, Skills and Abilities A thorough working knowledge of quality systems and Good Manufacturing Practices including Good Documentation Practices. Experience in Quality Systems Auditing against recognized Medical Device/Pharmaceutical Manufacturing Standards. Experience in supporting regulatory audits from US Regulatory Authorities. Experience with MasterControl, SAP, Share Point, Teamcenter, eCTR. Must have effective problem solving and interpersonal skills. Ability to read, write and follow verbal and written instructions. Ability to work independently, multi-task and thrive in fast-paced environment. Excellent written and verbal communication skills. Proficient in statistical software, Windows OS, Microsoft Office Suite including Word, Excel, and Power Point. Ability to make and implement decisions based on experience and facts as well as provide direction to peers or less experienced team members. Must have excellent communication and written skills. Able to be aware of all relevant standard operating procedures as per Company policy as they are related to the position covered by this Job Description. Support and contribute to Lean Sigma programs and activities towards delivery of the set target. Able to comply with the company’s safety policy at all times Able to comply with the company’s quality policy at all times. Travel Requirements 5%: Up to 13 business days per yearPhysical Requirements Sedentary-Exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time. West embraces diversity and equality of opportunity. We foster an environment where all individuals are safe, treated fairly, valued and respected. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, disability status or other applicable legally protected characteristics. Where permitted by law, employment with West Pharmaceutical Services, Inc. or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of post-offer background screening.  #LI-9394

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Responsibilities

The Document Control Specialist manages documentation systems to ensure compliance with regulatory requirements and internal procedures. They are responsible for batch review and release processes, as well as executing transactions in GMP systems like MasterControl and SAP.