Compliance Specialist - Risk Management
Newark Metro Area, NJ
The Compliance Specialist, Equipment Commissioning & Qualification supports the successful operation of facility, laboratory and business functions at multi use sites through interaction with internal team members and peer level customers as well as external service providers. The incumbent in this individual contributor role ensures the compliance of equipment and the ECQ group with local, global and regulatory guidelines. The incumbent will perform periodic reviews of equipment, policies and procedures, gap analysis where required, and small scale projects in order to complete departmental objectives.
1) Historical Performance Review:
a. Execute the historical performance review (HPR), a bi annual review of equipment performance and use.
b. Compile data gathered from HPR and use to analyze trends that could show equipment failure or out of trend.
c. Review equipment logbooks, procedures and use for adherence to local, global and regulatory policies, procedures and guidelines.
d. Identify and recommend actions to take as a result of the completed HPR.
2) Ensure ECQ Departmental Compliance:
a. Participate in revisions to departmental procedures to ensure compliance.
b. Ensure departmental procedures and policies comply with latest versions of local, global and regulatory policies, procedures and guidelines.
3) Compliance Projects:
a. Through job functions listed above identify and scope projects of small and large complexity required to keep equipment or the department in compliance.
b. Lead projects both small and large in scope required to keep equipment or the department in compliance.
Advanced knowledge of cGMP, GXP, GAMP, SDLC regulations, including 21CFR part 11, computer systems validation requirements and good documentation practices.
Advanced knowledge of pharmaceutical, manufacturing and laboratory systems and equipment.
Strong attention to detail.
Strong written and verbal communication skills.
Excellent interpersonal skills with experience dealing with a diverse workforce.
Strong multi tasking ability in conjunction with proven organizational skills. Ability to organize assigned tasks in a high paced environment and concurrently monitor tasks / assignments with others that may impact timely completion. Ability to effectively manage multiple tasks and activities simultaneously.
Strong presentation development and delivery skills.
Highly proficient computer skills in Microsoft Office Suite Word, Excel, PowerPoint and Outlook with extensive background in database systems. Innate ability to learn new software, such as corporate intranet and enterprise business.
Ability to organize and present data and findings clearly
Action and detail oriented
Team Player / Building Relationships
Education & Experience:
BS in Engineering or Science related discipline.
Minimum 5 years experience in GMP environment / regulated industr.y
2-3 years experience in a pharmacopeia compliance related discipline preferred.
2-3 year' experience with troubleshooting complex laboratory equipment.
Working knowledge of regulatory guidelines such as FDA, EMA, USP, EP and JP.
Excellent computer skills including knowledge of equipment data quality systems.
Strong verbal and written communication skills, and the ability to work independently.
Must have strong interpersonal and communication skills, be a team player and be willing to work in an environment where individual initiative, accountability to the team, and professional maturity are required