Actalent
Sr QC Chemist
Relocation offered - Shift: 8-5/8:30-5:30 M-F. Occasionally weekend work required (delay in production, in-process sample coming
rare). Two facilities, 10 minutes apart. MUST HAVE: Bachelor's degree in Chemistry, Biochemistry, or related scientific discipline (Master's or Ph.D. preferred). Minimum of 7 years of experience with a bachelor's degree, 5 years with a master's degree or 1 year with a PhD in a QC laboratory within the pharmaceutical, biotechnology, or chemical industry, with at least 3 years in a leadership role. Strong knowledge of analytical techniques such as GC, HPLC, KF, FTIR, water content, UV-Vis, titration, wet chemistry, analytical balances, and pH meters. Know how to validate or qualify pharmaceutical test measures (Med device)
test or chemical radiance (small molecules). Experience from large molecules and validation. Tested drug products for API. Experience writing reports & SOPs. Testing and validating at the same time. GMP experience. Description We are seeking a highly skilled and experienced Quality Control Chemistry Manager to lead and oversee the QC Chemistry team. This role is responsible for ensuring the integrity, accuracy, and compliance of all chemical testing activities in support of manufacturing and product release. The ideal candidate will bring strong leadership, technical expertise, and a deep understanding of cGMP regulations within a pharmaceutical or life sciences environment. Independent execution of various standard laboratory techniques, including but not limited to HPLC, LC/MS, GC, GC/MS, FTIR, KF, LOD, and appearance assessment. Independent preparation of samples, solutions, instrument set-up and breakdown. Lead the transfer of analytical methods to QC from internal and external sources. Analysis of various sample types with approved prescribed test methods. Provide guidance and support on day-to-day tasks to QC personnel. Represent the Quality Control Department on internal and external matters as requested by QC Manager. Independent authoring, reviewing, and execution of analytical method validation protocols. Lead internal meetings as requested. Independent authoring, reviewing, and execution of stability study protocols. Independent preparation of data packets, stability reports, and certificates of analysis to summarize analytical testing. Participation in, or lead, Out of Specification investigations and the documentation of analytical deviations along with qualified investigators and management. A working knowledge of QC laboratory operating under US FDA/EU GMPs. Provide mentorship to co-workers as needed. Skills Quality control, HPLC, GMP, pharmaceutical, GC-MS, GC/MS, LC-MS. Experience Level Intermediate Level. Pay and Benefits The pay range for this position is $43.00 - $60.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: Medical, dental & vision
Critical Illness, Accident, and Hospital
401(k) Retirement Plan
Pre-tax and Roth post-tax contributions available
Life Insurance (Voluntary Life & AD&D for the employee and dependents)
Short and long-term disability
Health Spending Account (HSA)
Transportation benefits
Employee Assistance Program
Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Eugene, OR. Application Deadline This position is anticipated to close on Sep 2, 2025.
Relocation offered - Shift: 8-5/8:30-5:30 M-F. Occasionally weekend work required (delay in production, in-process sample coming
rare). Two facilities, 10 minutes apart. MUST HAVE: Bachelor's degree in Chemistry, Biochemistry, or related scientific discipline (Master's or Ph.D. preferred). Minimum of 7 years of experience with a bachelor's degree, 5 years with a master's degree or 1 year with a PhD in a QC laboratory within the pharmaceutical, biotechnology, or chemical industry, with at least 3 years in a leadership role. Strong knowledge of analytical techniques such as GC, HPLC, KF, FTIR, water content, UV-Vis, titration, wet chemistry, analytical balances, and pH meters. Know how to validate or qualify pharmaceutical test measures (Med device)
test or chemical radiance (small molecules). Experience from large molecules and validation. Tested drug products for API. Experience writing reports & SOPs. Testing and validating at the same time. GMP experience. Description We are seeking a highly skilled and experienced Quality Control Chemistry Manager to lead and oversee the QC Chemistry team. This role is responsible for ensuring the integrity, accuracy, and compliance of all chemical testing activities in support of manufacturing and product release. The ideal candidate will bring strong leadership, technical expertise, and a deep understanding of cGMP regulations within a pharmaceutical or life sciences environment. Independent execution of various standard laboratory techniques, including but not limited to HPLC, LC/MS, GC, GC/MS, FTIR, KF, LOD, and appearance assessment. Independent preparation of samples, solutions, instrument set-up and breakdown. Lead the transfer of analytical methods to QC from internal and external sources. Analysis of various sample types with approved prescribed test methods. Provide guidance and support on day-to-day tasks to QC personnel. Represent the Quality Control Department on internal and external matters as requested by QC Manager. Independent authoring, reviewing, and execution of analytical method validation protocols. Lead internal meetings as requested. Independent authoring, reviewing, and execution of stability study protocols. Independent preparation of data packets, stability reports, and certificates of analysis to summarize analytical testing. Participation in, or lead, Out of Specification investigations and the documentation of analytical deviations along with qualified investigators and management. A working knowledge of QC laboratory operating under US FDA/EU GMPs. Provide mentorship to co-workers as needed. Skills Quality control, HPLC, GMP, pharmaceutical, GC-MS, GC/MS, LC-MS. Experience Level Intermediate Level. Pay and Benefits The pay range for this position is $43.00 - $60.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: Medical, dental & vision
Critical Illness, Accident, and Hospital
401(k) Retirement Plan
Pre-tax and Roth post-tax contributions available
Life Insurance (Voluntary Life & AD&D for the employee and dependents)
Short and long-term disability
Health Spending Account (HSA)
Transportation benefits
Employee Assistance Program
Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Eugene, OR. Application Deadline This position is anticipated to close on Sep 2, 2025.