Quality Control Specialist

Description We are hiring for a growing Contract Development and Manufacturing Organization (CDMO) based in Indianapolis, Indiana, and production locations in South Bend, IN; Bunker Hill, IN. We are seeking an experienced Quality Control Specialist to join our growing company. The Isotope Production Specialist will be responsible for process manufacturing of radiopharmaceutical products, preparation of production materials, supplies, and general production equipment maintenance. Job Duties: • Carries out production responsibilities to meet manufacturing schedules. • Performs chemistry manipulations for production in a GMP environment. • Ensure regulatory compliance of production protocols within the manufacturing operations. • Analytical methods and procedures for testing GMP manufactured radiopharmaceutical products. • Prepare and submit required reports. • Supporting and executing deviation reports, OOS, root cause investigations and CAPA. • Optimize and validate methods and procedures for radiopharmaceutical products. • Assist with creating SOPs for use in production. • Assist with the preparation of regulatory submissions. • Assist with general lab cleaning, supplies and maintenance. • Assist with waste management. • Performs other related duties as assigned. Skills Laboratory, Chemistry, Quality Control, Radiopharmaceutical, Nuclear Medicine, Radiopharma, HPLC, GMP, Isotope, Radioactive, Cyclotron, Pharmaceutical, Aseptic, Cleanroom, Troubleshooting, Lab Equipment, Instrumentation, Validation, Instrument Qualification, Calibrate, Radiation, Radiation Safety, Particle Accelerator, Isolator, RLT, Agilent Top Skills Details Laboratory Additional Skills & Qualifications Must Have: • An associate’s degree in chemistry, biochemistry, chemical engineering, or a related field, along with a minimum of 2 years of related experience in a pharmaceutical manufacturing environment (with preference to radiopharmaceuticals) may be considered. • Prior experience in pharmaceuticals, preferably in a quality or production position, is ideal. • Prior experience in a radiopharmaceutical environment a plus. • Excellent communication, analytical, computer/PC and technical writing skills. • The ability to handle responsibilities in a fast-paced manufacturing environment. • Demonstrated ability to work as part of a team. • Thorough understanding of project management. • Excellent organizational skills and attention to detail. Experience Level Intermediate Level
Job Type & Location
This is a Contract to Hire position based out of Indianapolis, IN.
Pay and Benefits
The pay range for this position is $30.00 - $35.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors. 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 Indianapolis,IN.
Application Deadline
This position is anticipated to close on Oct 2, 2026. 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

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 [email protected] for other accommodation options.

San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.

Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.