(QA/QC) in batch record deposition

QA/QC In Batch Record Deposition

Pay Rate: $40/HR on W2

Location: West Point, PA 19486

MUST HAVE:

• Prefer quality experience (QA/QC) in batch record deposition.
• Operations in packaging clinical supplies.
• Previous SAP is nice to have.
• Veeva is nice to have.

Qualifications:

Education: Bachelor's Degree or higher in engineering, science, or related discipline.

Required skills and experience:

• Minimum 2 years of experience in the pharmaceutical or equivalent industry, Good Manufacturing Practice (GMP) related field including Technical, Engineering, Quality or Operations.
• Familiarity with batch disposition activities
• Strong problem-solving, and written and oral communication skills
• Ability to manage multiple priorities
• Demonstrated teamwork skills and ability to work independently
• Proficiency in the use and maintenance of Microsoft applications (Excel, Outlook, and/or MS Access, Teams)
• Attention to detail, flexibility and an awareness of production and quality control problems.

Preferred skills and experience:

• Proven ability to work independently and collaborate effectively as part of a team.
• Strong organizational, interactive, and time management skills.
• Computer skills; knowledge and competency in ERP/MES, SAP

Note:

Hybrid View email address on click.appcast.io, PA (3 days onsite)

Responsibilities:

Our department supports the release of clinical supply to global clinical trials.

Primary duties may include but are not limited to the following:

• Evaluation and disposition of clinical supply materials with the assurance that the materials were produced in conformance to all applicable policies/procedures of our Company and compliance with all governing regulations.
• Coordinate and/or support the preparation of procedures, processes and quality improvements.
• Completing projects to improve the performance of our processes, including continuous process improvements, and value capture projects that seek to improve yield, reduce cost, or lower our processing cycle times.
• Assists in the coordination of significant quality events including fact finding, investigation support
• Actively using and championing the use of Lean Six Sigma and our company's Production System (MPS) tools, both in problem solving and day-to-day operational activities.

Kindly share your resume with answers:

Q1: How many years of exp in quality experience (QA/QC) in batch record deposition.

Q2: How many years of exp in Operations in packaging clinical supplies

Q3: How many years of exp do you have in Veeve

Q4: How far you live from and how will you commute daily 770 Sumneytown Pike, West Point, PA 19486