Hello,
Hope you are doing well!!

This is Priyanka from Experis, a ManpowerGroup company has an exciting contract opportunity for one of our key clients, a Fortune 500 American global biopharmaceutical company that is engaged in the discovery, development, and manufacture of healthcare products.

I have a job very good opportunity for you, please go through the below job details and if you feel interested, please share your resume on

Job Title - QA Specialist II (ABBVJP00021670)

Duration - 6 months

Location - Mettawa, IL 60045

The Specialist Quality Systems is responsible for providing quality assurance support for some or all of the following manufacturing processes: pharmaceutical products, medical devices, combination products and biologics. Specific areas of support may include the Document Center, Device QA, Labeling, Validation, Training and CAPA. This position will ensure that all product, process or system related quality activities from raw material inspection through shipment of final product are in compliance with Corporate and governmental regulations.

Responsibilities:

• Assist with proper integration and support of quality regulations: drug, biologics, device and/or combination products.
• Assist project teams in planning, preparation, review and approval of quality documentation.
• Complete and route change requests for process document creation, maintenance, and implementation.
• Create quality system documentation and specifications with guidance from technical teams following approved templates and guidelines.
• Assist with or co-lead audits of documentation, facilities and equipment.
• Assist in the design of effective quality systems, procedures and/or processes within cross functional teams to ensure compliance as well as efficiency throughout our quality system.
• Perform assessments to determine compliance to processes and regulations to identify potential gaps and mitigate and implement improvements within our quality system.
• Participate in training and education programs for various aspects of quality assurance.

Qualifications:

• Bachelor's degree in chemistry, Pharmacy, Biology, Microbiology, Engineering, or other technical/ scientific area preferred.
• 3+ years' experience in quality assurance, quality oversight or relevant experience.
• Technical knowledge in as many of the following areas as possible: Quality, Regulatory, Process Sciences, Manufacturing Operations.
• Knowledge and familiarity with product, process, equipment, and facilities of pharmaceutical, biological or device related products preferred.
• Knowledge of QA systems and GMP compliance requirements including regulations and standards affecting device, biologics, and pharmaceutical products preferred.
• Experience working in both team setting and independently. Works well with manager guidance to complete tactical objectives while able to manage own time effectively.
• Strong oral and written communication skills needed.
• Excellent interpersonal skills a plus.
• Runs small projects to deliver tactical results.

INTAKE CALL NOTES

Years of experience/education and/or certifications required:

• Bachelor's Degree
• 3+ years' experience in quality assurance, quality oversight or relevant experience.

What are the top 3-5 skills requirements should this person have?

• Quality mindset
• MS Office (Excel-average experience)
• Knowledge of QA systems and GMP compliance requirements including regulations and standards affecting device, biologics, and pharmaceutical products preferred.
• Strong oral and written communication skills needed
• Experience working in both teams setting and independently. Works well with manager guidance to complete tactical objectives while able to manage own time effectively.

What is a nice to have (but not required) regarding skills, requirements, experience, education, or certification?

• Bachelor's degree in chemistry, Pharmacy, Biology, Microbiology, Engineering or other technical/ scientific area preferred.
• Knowledge and familiarity with product, process, equipment, and facilities of pharmaceutical, biological or device related products preferred

Work Schedule (Define days, # of hours)/ Is Overtime offered or required?

• Standard 40-hour workweek (start time 7, 8 or 9am)

Does this position offer the ability to work remotely on a regular basis or is it an on-site role?

• (Hybrid- 3 days onsite; 2 days remote) must be local- training is onsite)

Interview Process:

• 30-minute Video interview with Manager
• Possibly 2nd interview if needed.

Apply Now