Mindlance
Shift
Sunday to Thursday morning shift 9-5:30 PM
Responsibilities
Perform micro test methods as written to support product/material release.
Effectively perform a multitude of laboratory techniques with minimal error for which the employee will be trained.
Understand, implement, and maintain GMP with respect to laboratory records, procedures, and systems in accordance with procedural requirements.
Accept responsibility to complete assigned tasks as committed.
Support investigation writers and approvers to gather data.
Write or revise procedures with guidance.
Work under the guidance of a supervisor while managing own time to ensure timely completion of assigned duties.
Trend data to support trend reports.
Willingness to work weekends and holidays.
Top Skills
QC Micro experience – hands‑on lab testing and/or EM.
Hands‑on aseptic technique experience.
Hands‑on experience in biosafety hoods.
Attention to detail while running assays/tasks in the lab and while performing EM.
Good organizational skills, ability to prioritize workload, and thoroughness with excellent attention to detail.
Perform tasks with supervision guidance, taking responsibility for complying with GMP requirements.
Strong interpersonal and communication skills; maintaining good working relationships within and outside the department.
Adjusting quickly to new situations and reprioritizing to meet schedule demands in a continually changing work environment.
Knowledge of the LIMS system, specifically entering results.
Nice to Have
Knowledge of applicable regulations and standards affecting pharmaceutical products (e.g., USP, EP, JP pharmacopoeias, ICH guidelines, cGMP).
GMP and/or Clean‑Room experience.
Clean‑Room gowning proficiency.
Experience with cGMP documentation and record maintenance.
Comfortable standing for most of the shift and willingness to shuttle between client buildings; flexible to work (some) weekends and holidays.
Experience Level: 3‑5 years.
Experience & Education
BS in Biology or other life science required.
3‑5 years of experience in a GMP laboratory environment.
Required experience with cGMP documentation and record maintenance.
EEO Statement Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of – Minority, Gender, Disability, Religion, LGBTQI, Age, or Veterans.
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Responsibilities
Perform micro test methods as written to support product/material release.
Effectively perform a multitude of laboratory techniques with minimal error for which the employee will be trained.
Understand, implement, and maintain GMP with respect to laboratory records, procedures, and systems in accordance with procedural requirements.
Accept responsibility to complete assigned tasks as committed.
Support investigation writers and approvers to gather data.
Write or revise procedures with guidance.
Work under the guidance of a supervisor while managing own time to ensure timely completion of assigned duties.
Trend data to support trend reports.
Willingness to work weekends and holidays.
Top Skills
QC Micro experience – hands‑on lab testing and/or EM.
Hands‑on aseptic technique experience.
Hands‑on experience in biosafety hoods.
Attention to detail while running assays/tasks in the lab and while performing EM.
Good organizational skills, ability to prioritize workload, and thoroughness with excellent attention to detail.
Perform tasks with supervision guidance, taking responsibility for complying with GMP requirements.
Strong interpersonal and communication skills; maintaining good working relationships within and outside the department.
Adjusting quickly to new situations and reprioritizing to meet schedule demands in a continually changing work environment.
Knowledge of the LIMS system, specifically entering results.
Nice to Have
Knowledge of applicable regulations and standards affecting pharmaceutical products (e.g., USP, EP, JP pharmacopoeias, ICH guidelines, cGMP).
GMP and/or Clean‑Room experience.
Clean‑Room gowning proficiency.
Experience with cGMP documentation and record maintenance.
Comfortable standing for most of the shift and willingness to shuttle between client buildings; flexible to work (some) weekends and holidays.
Experience Level: 3‑5 years.
Experience & Education
BS in Biology or other life science required.
3‑5 years of experience in a GMP laboratory environment.
Required experience with cGMP documentation and record maintenance.
EEO Statement Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of – Minority, Gender, Disability, Religion, LGBTQI, Age, or Veterans.
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