What are the responsibilities and job description for the MCS Associate Quality Control – (JP10309) position at 3 Key Consulting?
Job Title: MCS Associate Quality Control – (JP10309)
Location: Thousand Oaks, CA. 91320
Employment Type: Contract
Business Unit: ATO Quality Control
Duration: 1 years (with likely extensions)
Notes: Onsite. Qualified candidates only need apply.
Rate: 20 - 25/hour
Posting Date: 05/20/2022
3 Key Consulting is hiring a MCS Associate Quality Control for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
Under general supervision, this position will perform routine procedures and testing in support of the lab. This position will be responsible for one or more of the following activities: - Performing routine laboratory procedures - Routine analytical testing - Documenting, computing, compiling, interpreting, and entering data - Maintaining and operating specialized equipment - Initiating and / or implementing changes in controlled documents. Must learn and comply with safety guidelines and cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems and laboratory logbooks.
Basic Qualifications:
Bachelor’s degree and 2 years of Quality Control, Quality Assurance or related experience
OR
Associate’s degree and 6 years of Quality Control, Quality Assurance or related experience
OR
High school diploma / GED and 8 years of Quality Control, Quality Assurance or related experience
Preferred Qualifications:
Why is the Position Open?
Supplement additional workload on team.
Top Must-Have Skill Sets:
Day to Day Responsibilities:
Performing routine laboratory procedures, such as sample testing per analytical methods or protocols. Perform preventative maintenance on equipment and support daily laboratory duties.
Employee Value Proposition:
The person in this role will work with 22 different molecules. You will be very hands on and see medicines go to patients. This position has great opportunities for growth.
Red Flags:
Phone screening followed by in-person interview.
We invite qualified candidates to send your resume to resumes@3keyconsulting.com. If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.
Location: Thousand Oaks, CA. 91320
Employment Type: Contract
Business Unit: ATO Quality Control
Duration: 1 years (with likely extensions)
Notes: Onsite. Qualified candidates only need apply.
Rate: 20 - 25/hour
Posting Date: 05/20/2022
3 Key Consulting is hiring a MCS Associate Quality Control for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
Under general supervision, this position will perform routine procedures and testing in support of the lab. This position will be responsible for one or more of the following activities: - Performing routine laboratory procedures - Routine analytical testing - Documenting, computing, compiling, interpreting, and entering data - Maintaining and operating specialized equipment - Initiating and / or implementing changes in controlled documents. Must learn and comply with safety guidelines and cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems and laboratory logbooks.
Basic Qualifications:
Bachelor’s degree and 2 years of Quality Control, Quality Assurance or related experience
OR
Associate’s degree and 6 years of Quality Control, Quality Assurance or related experience
OR
High school diploma / GED and 8 years of Quality Control, Quality Assurance or related experience
Preferred Qualifications:
- Ability to adhere to regulatory requirements, written procedures and safety guidelines
- Ability to evaluate documentation/data according to company and regulatory guidelines
- Ability to organize work, handle multiple priorities and meet deadlines
- Strong written and oral communication skills
- Must be detail orientated
- Must be flexible and adaptable to changing priorities and requirements
- Demonstrate understanding of regulatory requirements, safety guidelines and factors impacting compliance
- Demonstrates understanding of when and how to appropriately escalate.
- May identify, recommend and implement improvements related to routine job functions.
- Must learn and comply with safety guideline and cGMPs.
Why is the Position Open?
Supplement additional workload on team.
Top Must-Have Skill Sets:
GMP Experience or Lab Experience (Biology degree)
Day to Day Responsibilities:
Performing routine laboratory procedures, such as sample testing per analytical methods or protocols. Perform preventative maintenance on equipment and support daily laboratory duties.
Employee Value Proposition:
The person in this role will work with 22 different molecules. You will be very hands on and see medicines go to patients. This position has great opportunities for growth.
Red Flags:
- Non-biology-related degree
- No lab experience
Phone screening followed by in-person interview.
We invite qualified candidates to send your resume to resumes@3keyconsulting.com. If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.
