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Description

Responsible for acquiring the skills to inspect and accept/reject incoming raw packaging materials and components, monitor operational activities for compliance with cGMP and SOPs, work on semi-routine tasks where ability to recognize deviation from standard practice is required. This position also conducts QC activities within a specified timeline to meet customer requirements, interact with all levels of employees, customers, and assists QA personnel as necessary. This position uses database applications and standard precautionary procedures to work independently, be self-directed, communicate effectively, and use good judgement when making decisions. Internal or external client interaction occurs under the guidance of experienced professional or technical staff. QC Technician I duties: - Ensures the operations personnel adhere to SOPs and follow Batch Record instructions. - Approves and controls labels. - Reviews documents completed by operations personnel. - Resolves production/QC and documentation discrepancies. - Responds to inquiries on quality control activities and schedules in general. - Collects and trends Quality Control Data and maintains the QC Shipping & Receiving Logs. - Ensures all job related paperwork is correct, error-free, and entered into appropriate operating systems daily. - May be required to travel to other facilities to meet business needs.

Skills

gmp, Data Enrty, QC, Quality Control, Inspection, Production, Biological specimens, biological samples, Quality Control Data, quality control inspection

Top Skills Details

gmp,Data Enrty,QC,Quality Control,Inspection,Production

Additional Skills & Qualifications

1st shift 8am-5pm - Requires ability to communicate effectively verbally and in written form. - Requires ability to pay attention to detail/follow up. - Requires excellent interpersonal, problem solving and planning/organizational skills. - Requires knowledge of Windows and Microsoft office applications. - Requires ability to learn new computer systems quickly. - Requires ability to work independently and as part of a team. - Prefer proficiency in applications of 21 CFR Parts 11, 210, 211, and 820, as well as ICH 7 and 8 Requires HS Diploma, Life Science degree preferred. Prefer 1+ years of work experience with data entry and inspection. Prefer prior experience in pharmaceutical production or inspections (cGMPs). Prefer proficiency in cGMP requirements as they relate to holding and distributing finished pharmaceuticals and biological specimens. Prefer knowledge of Universal Precautions, general laboratory and quality assurance/control. Certificates and/or Licenses: -IATA Dangerous Goods Training for Class 6.2 Shipping. -Blood Borne Pathogens Training.

Experience Level

Entry Level

Pay and Benefits

The pay range for this position is $23.00 - $24.00/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 Rockville,MD.

Application Deadline

This position is anticipated to close on Oct 17, 2025.

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.

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 due to a disability, please email [email protected] (%[email protected]) for other accommodation options.