Core Technician I
Mindlance
Description:
The Core Technician is a scientist role and will be responsible for performing a variety of tasks associated with the production of sterile biological pharmaceutical products. Responsibilities:
Knowledgeable and complies with all pertinent safety policies, rules and regulations.
Ensure that all team members comply with safety rules and regulations.
Maintenance of quality systems and cGMP compliance for the business by ensuring that all team members comply with processes, procedures and instructions for all activities in which the team participates.
Able to perform procedures according to written guidelines and recognize a deviation from accepted practice.
A majority of the work is done in cleanroom environment.
While working in the cleanroom, scrubs, hairnet, shoe covers, hood, gown, mask, boots and two pairs of gloves are required.
Must be capable of motivating others, creating a positive work climate where inter-departmental collaboration, coaching and performance feedback are continuous.
Capable of clearly assigning objectives, clearly setting and measuring and monitoring progress, marshaling resources and handling competing priorities.
Experienced at establishing clear directions, leading others and bringing out their best. Education:
Bachelor's Degree in Life Sciences preferred. Basic Lab experience with a Bachelor's degree or Intermediate Lab experience within a cGMP clinical production environment and a High School Diploma.
Lab experience preferred.
1-3 Years Experience Shift
12 hour rotating shifts - 2 days on, 2 days off, 3 days on, 3 days off
Day shift: 7am-7:30pm shift
***MUST BE AVAILABLE TO TRAIN ON FIRST SHIFT - 5 days/ week for the first 4-6 weeks*** EEO:
"Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of - Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans."
The Core Technician is a scientist role and will be responsible for performing a variety of tasks associated with the production of sterile biological pharmaceutical products. Responsibilities:
Knowledgeable and complies with all pertinent safety policies, rules and regulations.
Ensure that all team members comply with safety rules and regulations.
Maintenance of quality systems and cGMP compliance for the business by ensuring that all team members comply with processes, procedures and instructions for all activities in which the team participates.
Able to perform procedures according to written guidelines and recognize a deviation from accepted practice.
A majority of the work is done in cleanroom environment.
While working in the cleanroom, scrubs, hairnet, shoe covers, hood, gown, mask, boots and two pairs of gloves are required.
Must be capable of motivating others, creating a positive work climate where inter-departmental collaboration, coaching and performance feedback are continuous.
Capable of clearly assigning objectives, clearly setting and measuring and monitoring progress, marshaling resources and handling competing priorities.
Experienced at establishing clear directions, leading others and bringing out their best. Education:
Bachelor's Degree in Life Sciences preferred. Basic Lab experience with a Bachelor's degree or Intermediate Lab experience within a cGMP clinical production environment and a High School Diploma.
Lab experience preferred.
1-3 Years Experience Shift
12 hour rotating shifts - 2 days on, 2 days off, 3 days on, 3 days off
Day shift: 7am-7:30pm shift
***MUST BE AVAILABLE TO TRAIN ON FIRST SHIFT - 5 days/ week for the first 4-6 weeks*** EEO:
"Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of - Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans."
Vacancy posted 4 days ago
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