QC Scientist (pharma/micro)

QC Scientist (pharma/micro)

Quality Control

Wilmington, OH, US

Pay Rate Low: 45 | Pay Rate High: 55

• Added - 14/08/2025

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Our client, a global leader in the pharmaceutical manufacturing industry, is seeking a experienced QC Scientist to join their team!

• Hours : 1st shift M-F (flexible to 7a-4p, 8a-5p, 9a-6p)

• Pay Rate: $45-55/hr

• Terms : 12-18 month contract (COULD go temp-to-hire)

• Ideal Candidate Profile: strong microbiology background (chemistry too is a plus) with a MS or PhD and pharmaceutical indsutry expereince!

QC Scientist I

Background

• Lead Team in project Coordination and support

• Coordinate and support Tech Services Projects, which include:

• Method Validations and optimizations

• New technologies and equipment

• Assist in the identification of new testing technologies and equipment to meet evolving regulatory requirements.

• Support regulatory audits.

• Write protocols and execute method verification/validation/qualification/ transfers

• Write, execute laboratory investigations for out of specifications and out of trend results

• Point person for higher level meetings / projects such as CMC Team support.

• Write documents (SOPs, specifications, technical reports)

• Execute, oversee instrument qualification as necessary.

• Implement continuous improvement activities to maximize the resources available

• Write change controls and work orders for systems and instrumentation changes

• Review data as needed utilizing LIMS, SAP and SLIM

• Troubleshooting of technical procedures, methodology and instrumentation

• Data entry for testing results following GMP regulations

• Review tests results for other analysts

• Train new analysts and document training

• Provide technical support to new analysts

• Participate in non-routine projects, validations and method development to meet departmental and individual goals

• Review SOPs, product specifications and controlled forms to comply with USP, EP, JP and CP regulations

• Maintain the laboratory operations in compliance with industry regulations

• Maintaining inventory of material and reagents for technical services

• The successful candidate will be responsible for managing their time, organizing their workload to be efficient, and have good organizational and communication skills. Qualifications

• BSc In science related field with (min) 10+ years experience in pharmaceutical manufacturing, MS degree with 3-5+ years of experience or PhD with 0-5+ years

• Able to work autonomously, receiving general instructions on new assignments.

• Strong technical knowledge of microbiological / Chemistry test instrumentation and method development / validation including software/computer system validation.

• Experience with the execution and validation of test methods for sterile and non-sterile drugs, their raw materials, components and in-process testing. This includes the methods described in USP Chapters and relevant informational chapters.

• Knowledge of current compendia requirements.

• Excellent organizational, planning and scheduling skills: Capable of managing/coordinating multiple projects and priorities in a dynamic environment while maintaining a professional demeanor.

• Critical, Fact-Based Decision Making: Demonstrates a systematic approach to problem solving; considers all relevant facts & data when making decisions; applies previous experience & best practices to new situations.

• Personally Accountable: Owns the results of their individual actions & team activities. Ability to learn from mistakes & holds a strong belief in continuous improvements, both personally & professionally.

• Agility: Able to quickly change direction when business priorities or customer requirements change; exhibits a high level of flexibility when confronted with new or unexpected circumstances

• Good verbal and written communication skills; confident presenter, clear, concise technical writer.

• Familiar with common MS Office software packages. Personal Attributes

• Motivated self-starter

• Team player

• Committed to quality

• Well organized, efficient worker

• Good problem solver

• Critical, analytical thinker

• Manages multiple duties and projects

• Creative, innovative thinker

• Easily adaptable to change

• Brings closure to work in a timely mannerThis job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!INDBH

We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.