qa consultant iii.

• pennington , new jersey

• posted 3 days ago

job details

summary

• $72.27 - $85.03 per hour

• contract

• bachelor degree

• category life, physical, and social science occupations

• reference49078

job details

job summary:

As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!

Location: Hopewell, NJ

location: Pennington, New Jersey

job type: Contract

salary: $72.27 - 85.03 per hour

work hours: 9 to 5

education: Bachelors

responsibilities:

Duties:

• This position is based in Hopewell, NJ. Supports QA manufacturing activities in the Warehouse, DS/DP production areas, QC Laboratories as well as Facility/Utility areas that support GMP manufacturing. Candidate will ensure the successful day to day management of reviewing and approving GMP paperwork including logbooks, analytical raw data, Environmental Monitoring reports, and other ancillary documentation that supports GMP Manufacturing. Works to support QA objectives whilst adhering to regulatory compliance and achieving business success. Creates and/or reviews SOPs needed to support the business. Works to support both internal GMP audits and Health Authority audits

qualifications:

Skills:

• Supports/participates in regulatory and customer inspections/audits as required.

• Maintaining and improving QA operational performance, to meet the requirements of regulatory authorities, company Standard Operating Procedures (SOPs) and external and internal customers.

• Implementing and monitoring all Quality Assurance activities in laboratories and facility/utility space to ensure compliance with FDA/EU regulations, covering cGMP for commercial medicinal products and clinical material for human use.

• Ensuring the QA Compliance of departmental SOPs (writing & revising), ensuring regulatory compliance in conjunction with being 'fit for purpose' operationally and commercially.

• Knowledgeable in cGMPs: 21 CFR Parts 11, 210, 211, and 600.

• Demonstrated expertise with ERP systems such as Maximo, Veeva, and SAP.

• Ensuring all activities are performed in accordance with GMPs, SOPs and Health and Safety policies.

• Awareness of USP/EP, ICH Guidelines, QC methodology updates to ensure compliance with current testing and specifications.

• Ensuring appropriate escalation and follow up for non-conformities within Laboratories and Utility areas, and issuing deviations when appropriate.

• Undertaking any other duties for any department within the business, which may be requested by Management, for which training and/or an explanation has been provided and understood.

• Credible and confident communicator (written and verbal).

• Customer focused, Strong analytical and problem-solving ability.

• Good project management skills.

• Hands-on approach, with a 'can do' attitude.

• Ability to prioritize, demonstrating good time management skills.

• Attention to detail, with the ability to work accurately & efficiently in a busy and demanding environment.

• Self-motivated, with the ability to work proactively using own initiative. Innovative thinker.

• Committed to learning and development.

• Highly Desirable: Good IT skills e.g., Microsoft Office (Word, Excel, PowerPoint, Project and Outlook)

Required Skills:

• CFR 21

• BIOTECH/PHARMACEUTICAL

• PHARMACEUTICAL QUALITY ASSURANCE

• CGMP/FDA

• ENVIRONMENTAL MONITORING

Additional Skills:

• SAP

• TIME MANAGEMENT

• DOCUMENTATION

• ICH

• QA

• USP

• MAXIMO

• SOPS

• CGMPS

• REGULATORY COMPLIANCE

• INSPECTIONS

• BIOTECHNOLOGY

• FDA

• PROBLEM-SOLVING

• ENTERPRISE RESOURCE PLANNING

• AUDIT

• CHEMISTRY

• EXCEL

• PROJECT MANAGEMENT

• PHARMACY

• MICROSOFT POWERPOINT

• CGMP

• EXCELLENT WRITTEN AND VERBAL COMMUNICATION SKILLS

• QUALITY ASSURANCE

• QUALITY CONTROL

Education

• Bachelors Scientific degree (ideally biotechnology, biology, pharmacy, pharmaceutical sciences, chemistry or related scientific field) or equivalent work experience.

• Required 3+ years (B.S. degree) or 1 years (M.S. degree) of GMP Pharmaceutical experience working in a quality assurance or quality control role in an FDA-regulated company.

• Working knowledge of cGMPs: 21CFR parts 11, 210 & 211, knowledge of 21CFR600 - Biologics desirable.

skills: Quality control, FDA, Quality Assurance, GMP (Good Manufacturing Practice)

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).

This posting is open for thirty (30) days.