Sr. QC Tech (Pharma)

HIRING: Sr. Quality Control Tech (Pharmaceutical Experience

Summary:

Supporting one of the world’s largest nuclear medicine company that manufacture and distribute world-class radiopharmaceutical products to help patients around the globe. Perform assigned laboratory testing and related quality control activities in order to ensure compliance with applicable SOP's and cGMPs. Provide timely testing and notification of any aberrant occurrence to Management/Supervision that presents potential negative impact to manufactured or marketed product. Training and development will be thoroughly provided.

Essential Responsibilities:

• Ensure a safe and quality working environment through training, awareness, and compliance to Safety/Quality guidelines and SOPs.
• Analytical Method Validation and Verification (USP Compendial and Non-Compendial)
• Analytical Equipment IOQ
• Ensure the maintenance of the Analytical department, premises, and equipment.
• Ensure that all necessary training is carried out to perform all the assigned tasks confidently and consistently.
• Perform all work in compliance with site safety and radiation protection guidelines.
• Collaborate with other team members to ensure that quality tasks are performed in a timely manner.
• Must demonstrate flexibility in adjusting to changing priorities and schedules.
• Attend mandatory trainings as required by site regulatory requirements and management.
• Assist with investigations by providing testing results and communication of practice(s).
• May supervise the work of others and coordinate instrumentation use and completion of laboratory testing.
• Work under limited supervision with considerable latitude for the use of initiative and independent judgment.

Qualifications Required:

• Bachelor's or Master's Degree in Life Science
• 3+ years of analytical chemistry experience (HPLC, GC, or ICP most relevant)
• 2+ years of quality/lab experience within regulated industry or GMP facility (pharma preferred)
• Preferred but Not Required - Method development/validation experience
• Preferred but Not Required - Relevant instrumentation experience with Analytical Balance, pH Meter, Automatic Pipettes, FTIR, UV-Vis, Voltammeter, Autotitrator, HPLC, GC, IC, ICP, Flame AA, TOC, Conductivity Meter.
• Skills: Quality Control, Method Validation, Chemistry, Method Development, Analytical, cGMP, HPLC, GC, GC-MS, GCMS, ICP, Laboratory, Aseptic, Pharmaceutical, Radiopharmaceutical

Miscellaneous:

• Company is continuously growing with a national footprint.
• Candidates will have the chance to learn Leadership responsibilities and be looked at as a true leader.
• This team is very Employee-Focused with Competitive Incentives and career pathways.
• Benefits: National Paid Holidays, Dental, Vision, Health, 401k Savings, Employee Assistance and Abenity program, PTO

INTERESTED IN THIS ROLE? Apply TODAY for immediate consideration:

• We are actively hiring and interviewing for this position and I will be conducting phone interviews as early as today. All candidates will be considered within 24 hours of reaching out directly to Grace Williams.
• HOW TO APPLY: Email your updated resume, brief intro about your interest, preferred method of communication for you (i.e., call, email, text) to grawilliams@actalentservices. com or call (317-567 -6610) 

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

• Hiring diverse talent
• Maintaining an inclusive environment through persistent self-reflection
• Building a culture of care, engagement, and recognition with clear outcomes
• Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.