29 days old

Quality Specialist, Date Integrity, OeC

Kelly Services
Riverview, MI 48193
**Kelly Services is actively recruiting for a Quality Specialist, Data Integrity, QeC for a Direct Hire opportunity in the Greater Detroit area, MI.**

**Customer Job Title:** Quality Specialist, Date Integrity, QeC

**Job Description:** POSITION SUMMARY: Quality Specialist - Data Integrity and QeC is responsible for the administration and coordination of the sites Data Integrity compliance, QeC and equipment/facilities qualification review and approval to meet end-user needs and regulatory expectations (21 CFR Part 11 and cGMP), and established SOPs.

To perform this position successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required:

Shall adhere to all applicable regulatory requirements, including FDA, EPA, OSHA, ICH and related safety, health and environmental procedures, policies and practices.

Consistent support and practice of all the Clients mission, vision, and values.

Identify and protect the original technical information as part of the company property.


Data Integrity Compliance Officer (DICO), lead gap assessments of new and existing systems/practices; perform DI risk assessments for identified gaps; perform DI Audits of site; provide timely update on DI plan to Central DICO; and ensure site team is trained on DI aspects and requirements.

To define validation strategy and review CSV deliverables for Site IT projects e.g. URS, FRS, CS, IQ, OQ, PQ, RTM, VSR, Risk assessment, etc. for applications installed at Riverview Site.

To define equipment/facilities qualification strategy and review Validation Department deliverables for Site equipment/facilities qualification e.g. URS, FRS, IQ, OQ, PQ, Risk assessment, drawings etc. for equipment/facilities at Riverview Site.

To have thorough understanding, practical approaches for Computer system validation (CSV) of applications.

Author, review and approval of SOPs, Guidelines/Policies as applicable to CSV, DI and equipment/facilities qualification.

To perform periodic and audit trail review of computerized systems as per defined frequency.

To support the initiatives undertaken by Corporate Quality eCompliance team in Riverview Site.

Ability to represent during regulatory audits.

Accountable to ensure compliance of CSV documentation and qualification during various phases (project, operational & retirement) of software lifecycle (SLC) and equipment/facilities.

Well aware with GAMP5, CFR Part 11/EU Annex 11, Data integrity and ICH Q7 requirements.

To ensure infrastructure (Network, Servers, Cloud, Database)and equipment/facilities are qualified as per required Quality standards and required documents are in place.

To review QMS documents e.g. Change control/Deviation/Incidents-Discrepancy/User access forms

To review and approve Root cause analysis and CAPA based on QMS documents.

To guide and train Site IT & Business teams at Site for CSV, Data Integrity and Regulatory Compliance activities.

To work along with CSV, Engineering & Project Manager to ensure project timelines are met.

Review, approve and ensure compliance of the implementation, maintenance, and update of existing drawings from as-designed to as-built as appropriate for equipment/facilities.

Ensure compliance and review/approve of site Validation Master Plan to include all GMP systems used at the site, including schedules for periodic review and as required, equipment/system requalification.

Guide and mentor site teams on compliance of IT and electronic systems.

Stay up to date on advances in the software and technology; provide appropriate training to new and current employees as needed.


Bachelors degree in Chemistry or life sciences. A minor in computer sciences is desirable.

More than five (5) years of relevant experience.


Excellent written and oral communication. Present and train relevant information to all levels within the company.

Ability to adapt to and thrive in a dynamic work environment and cooperate with employees and clients from a broad range of disciplines and subject-level expertise.

Demonstrated ability to multi-task on ongoing projects and tasks.

To have in depth understanding of regulatory requirements and guidelines required to comply IT systems in Pharma industry DI, Part 11, Annex 11, GAMP 5 etc.

Knowledge of Pharma domain Manufacturing and Quality (QA, QC)

Experience of working on Pharma Manufacturing Site and functional knowledge about chromatography systems, SCADA, DCS etc.

Understanding and exposure to Pharma CSV upcoming trends.

Knowledge about Good documentation practices, DI and ALCOA Knowledge and experience on handling of QMS e.g. Change control, deviation and incidents.

Knowledge and experience in equipment/facilities qualification


The physical demands and work environment described here are representative of those that must be met by a team member to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Physical Demands:

o Frequent lifting, bending, stooping, squatting, pushing and pulling can be expected.

o Long periods of standing and walking can be expected in this position.

o This position may require long periods of sitting, typing, computer entry or looking at a computer.

**If you feel you have the knowledge and expertise, apply today to connect with a Kelly professional who will work to enrich your life.**



**You should know:** Your safety matters! Vaccination against COVID-19 may be a requirement for this job in compliance with current client and governmental policies. A Kelly recruiter will confirm and share more details with you during the interview process.

**Why Kelly** **** **Science & Clinical?**

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the worlds most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goalsits the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

**About Kelly** ****

At Kelly, were always thinking about whats next and advising job seekers on new ways of working to reach their full potential. In fact, were a leading advocate for temporary/nontraditional workstyles, because we believe they allow flexibility and tremendous growth opportunities that enable a better way to work and live (plus, did we mention we provide a ton of benefits ?). Connecting great people with great companies is what we do best, and our employment opportunities span a wide variety of workstyles, skill levels, and industries around the world.

Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kellys Human Resource Knowledge Center.
Kelly complies with the requirements of Californias state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.
Posted: 2022-08-29 Expires: 2022-10-03

Before you go...

Our free job seeker tools include alerts for new jobs, saving your favorites, optimized job matching, and more! Just enter your email below.

Share this job:

Quality Specialist, Date Integrity, OeC

Kelly Services
Riverview, MI 48193

Join us to start saving your Favorite Jobs!

Sign In Create Account
Powered ByCareerCast