QC Scientist (pharma/micro)
Quality Control
Wilmington, OH, US
Pay Rate Low: 45 | Pay Rate High: 55
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 manner
This 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
Quality Control
Wilmington, OH, US
Pay Rate Low: 45 | Pay Rate High: 55
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 manner
This 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
Job ID: 489538955
Originally Posted on: 8/15/2025
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