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manufacturing associate - gmp

In Massachusetts United States

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manufacturing associate - gmp   

JOB TITLE:

manufacturing associate - gmp

JOB TYPE:

Full-time

JOB LOCATION:

Cambridge Massachusetts United States

JOB DESCRIPTION:

Moderna is seeking a cGMP Manufacturing Associate for mRNA Manufacturing.
This position is located at our the manufacturing site in Cambridge, MA.
The individual in this role will be part of a cohesive team responsible for producing GMP mRNA-based medicines for evaluation in human clinical trials.
He/she will apply existing and new knowledge of bioprocess unit operations and cGMPs to enable technical success with stringent adherence to a Quality System that respects global regulatory expectations.
The successful candidate will be able to document and communicate their technical and operational observations clearly and efficiently.
They will be able to operate pilot-scale bioprocessing equipment and interact fluidly with peers and supervisors in Manufacturing, and cross-functionally with Quality Control, Quality Assurance, Logistical and Process Development Technology Transfer counterparts.
The anticipated time frame for this assignment is six months.
There are multiple shifts available!

salary: $30 - $40 per hour
shift: First
work hours: 8 AM - 8 PM
education: Bachelors

Responsibilities
  • Execute manufacturing operations using disposable technologies, automation, and
  • Manufacturing Execution Systems (MES) to produce mRNA
  • Closely partner with QA peers for rapid disposition of mRNA
  • Demonstrate general knowledge of standard manufacturing practices and equipment.
  • Strict adherence to current good manufacturing practices, standard operating procedures, and
  • manufacturing documentation.
    Establish and follow written procedures for the clear and
  • accurate documentation of equipment operation and process instructions, and of process data.
  • Monitor process operations to ensure compliance with specifications.
  • Assist in the investigation of procedural deviations.
  • Practice safe work habits and adhere to Modernas safety procedures and guidelines.
  • Utilize knowledge to improve operational efficiency.
  • Adhere to gowning procedures and maintain a clean general operating area.
  • Adhere to documented waste handling procedures to respect environmental regulations.
The essential functions of this role include:
  • working weekends
Skills * GMP
  • Biotech
Qualifications * Years of experience: 3 years
  • Experience level: Experienced
Randstad is a world leader in matching great people with great companies.
Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company.
Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.


Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.


At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants.
If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.
com.


Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc.
In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).


Applications accepted on ongoing basis until filled.

randstadusa.
com\"> Randstad

Position Details

POSTED:

EMPLOYMENT:

Full-time

SALARY:

40 per year

SNAPRECRUIT ID:

S-1707129528-fa7475afb14aa328638a82a862a3f11a

LOCATION:

Massachusetts United States

CITY:

Cambridge

Job Origin:

jpick2

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In Dallas Fort Worth
Aug 19, 2017 9am-6pm
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Moderna is seeking a cGMP Manufacturing Associate for mRNA Manufacturing. This position is located at our the manufacturing site in Cambridge, MA. The individual in this role will be part of a cohesive team responsible for producing GMP mRNA-based medicines for evaluation in human clinical trials. He/she will apply existing and new knowledge of bioprocess unit operations and cGMPs to enable technical success with stringent adherence to a Quality System that respects global regulatory expectations. The successful candidate will be able to document and communicate their technical and operational observations clearly and efficiently. They will be able to operate pilot-scale bioprocessing equipment and interact fluidly with peers and supervisors in Manufacturing, and cross-functionally with Quality Control, Quality Assurance, Logistical and Process Development Technology Transfer counterparts. The anticipated time frame for this assignment is six months. There are multiple shifts available!

salary: $30 - $40 per hour
shift: First
work hours: 8 AM - 8 PM
education: Bachelors

Responsibilities
  • Execute manufacturing operations using disposable technologies, automation, and
  • Manufacturing Execution Systems (MES) to produce mRNA
  • Closely partner with QA peers for rapid disposition of mRNA
  • Demonstrate general knowledge of standard manufacturing practices and equipment.
  • Strict adherence to current good manufacturing practices, standard operating procedures, and
  • manufacturing documentation. Establish and follow written procedures for the clear and
  • accurate documentation of equipment operation and process instructions, and of process data.
  • Monitor process operations to ensure compliance with specifications.
  • Assist in the investigation of procedural deviations.
  • Practice safe work habits and adhere to Modernas safety procedures and guidelines.
  • Utilize knowledge to improve operational efficiency.
  • Adhere to gowning procedures and maintain a clean general operating area.
  • Adhere to documented waste handling procedures to respect environmental regulations.
The essential functions of this role include:
  • working weekends
Skills * GMP
  • Biotech
Qualifications * Years of experience: 3 years
  • Experience level: Experienced
Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).

Applications accepted on ongoing basis until filled.

Randstad


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