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Quality Control Chemist

1 month ago

Marion, United States DivIHN Full time
Job DescriptionJob Description

Title:  Quality Control Analyst (2 - Openings)

Location: Marion, NC

Duration: 12 Months

 

Description:

 

Confirmed 12 hours shift:

Day: 7:00 PM to 7:00 AM

2-2-3 rotation

2 days on, 2 off, 3 on, and then 2 off, 2 on, 3 off from FG

 

Summary of Position:

·        Perform Quality Control analyses according to Client procedures which include Specifications, Test Methods, Standard Operating Procedures (SOPs), Pharmacopoeia (USP, EP & JP) requirements, and current Regulatory guidelines promptly to support production processes, following instructions according to the supervisor or designee request.

·        Looking for a person having 1-2 years of relevant experience, some analytical expertise, and HPLC, ISPMS or related techniques knowledge. They need to support analytical testing, so looking for who can identify the test methods, and method development background is a plus.

·        Sometimes they have to work in the evening and on weekends for lab tasks.

·        They have to show up to work, as per the schedules.

·        Nice to have experience in reading and writing investigations.

 

Essential Duties and Responsibilities:

·        Perform analysis by Client Specifications, Test methods, SOPs, USP, EP, and JP Procedures; comply with current regulations and requirements (e.g. cGMP, cGLP, cGDP, etc); follow all Safety rules applicable to lab analyst work duties.

 

Experienced performing instrumental analysis on at least 3 of the following techniques:

·        HPLC, Atomic Absorption, Flame Photometry, ICP-MS, Polarimetry.

·        Prepare and submit accurate and timely analysis reports for all laboratory work.

·        Prepare and standardize solutions.

·        Practice Proper laboratory housekeeping procedures as per specified by the established procedures and GLP's.

·        Conduct the analytical testing, and release of raw materials and packaging components as required.

 

Conduct all assigned tasks in a safe way and in compliance with the following:

·        Test methods and SOP requirements, SDS handling and precautions, Federal and state legislated requirements (OSHA, EPA, FDA, EP, etc), and Company requirements (safety rules and policies).

·        Analyze complaint and Stability samples in a timely and accurate manner; report any quality issue to the lab Manager or designee

 

Assure analytical results are neat and accurate.

 

Regulations:

·        Basic cGMP knowledge.

 

Technical Qualifications and Other Background:

·        Computer literate (Word, Excel, PowerPoint)

·        Experienced using lab data systems such as Empower, Mass Hunter, LIMS, and Electronic Lab Notebooks

·        Ability to operate laboratory testing equipment

·        Must be able to work rotating shifts, weekends, and holidays.

·        Able to interpret and convert units of measure such as temperature, pressure, flow, area, mass, distance, volume or other.

·        Mathematical Reasoning: Add, subtract, multiply, divide and calculate percentages as well as able to use a calculator or other associated electronic equipment.

·        Ability to follow written procedures and/or verbal instructions, communications by telephone, fax or shortwave radios.

·        Potential for temp to hire opportunity based on performance.

·        No language preferences, English is fine.

 

Top requirements:

·        Professional exp in analytical chemistry, routine testing, understanding of analytical chemist duties and techniques, working on computers, working on software, managing HPLC.

 

Education:

·        Bachelor's Degree in Chemistry (Required)

·        If an individual has a good no. of experience in relevant fields then AS degree is also considerable.

·         

Job Experience:

·        2-minimum in professional analytical chemistry role.

 

Possibility of extension or conversion: Yes

 

Interview: Group interview with 3-4 members, 1 interview – Virtual.