Summary of Position
The Manufacturing Associate I participates in the manufacturing of biopharmaceutical drug product to support MacroGenics multiple clinical programs in the Cell Culture area. This position will work in the manufacturing suite under GMP (Good Manufacturing Practices) to ensure that materials manufactured meet required specifications and regulatory requirements.
Responsibilities and Job Duties
- Participate in hands-on production in the manufacturing of material for clinical trials in a GMP environment including operating expansion and production reactors conducting harvest operations and ordering and accounting for consumption of raw materials and components.
- Contribute to the creation and revision of Batch Records Work Instructions Standard Operating Procedures Material Specifications and other GMP documents
- Adhere to all SOPs and execute batch records under GMP regulations documenting all manufacturing activities clearly and accurately including preparation records testing records equipment use records and laboratory notebooks
- Maintain adequate supplies and perform routine equipment maintenance
- Maintain manufacturing area in a clean neat and orderly condition at all times
- Participate in a variety of projects designed to improve the quality and efficiency of the manufacturing team
- Follow all related safety rules and procedures when working with hazardous materials
Qualifications
Education & Experience
- High School Diploma or equivalent with exposure to science and math coursework and a minimum of two years of related biopharmaceutical manufacturing experience in FDA regulated controlled production environment
OR
- Associates degree with one year of related biopharmaceutical manufacturing experience in FDA regulated controlled production environment
OR
- Bachelors degree in a related discipline with no experience
Knowledge Skills and Abilities
- Knowledge of cell culture techniques
- Ability to write and revise technical documents
- Ability to lift up to 30 lbs.
- Ability to work occasional weekends or overtime as needed
- Ability to follow detailed instructions and to maintain accurate records and notes
- Ability to work effectively in a team environment
- Ability to successfully perform multiple tasks when required
- Skills in problem solving and troubleshooting
- Ability to safely operate production equipment in accordance with established practices
Supervisory Responsibilities
None
Preferred Qualifications
- Previous GMP experience
- Ability to use MS Office (Word Excel)
Additional Information
The annual equivalent of pay for the Manufacturing Associate I position ranges from $47250 - $78750. For non-exempt roles and according to applicable regulations there may be the possibility for overtime pay. This role is eligible for the Companys discretionary bonus and discretionary equity incentives. Eligible employees may participate in the Companys benefits programs including medical / dental / vision / prescription coverage employee wellness resources 401(k) plan with employer match access to an Employee Stock Purchase Plan (ESPP) paid time off & paid parental leave benefits and disability benefits.
The annual pay rate range is described in good faith and the Company believes is the range of possible compensation for this role at the time of this posting depending on the candidates experience qualifications geographic location and other factors permitted by law. The Company may ultimately pay more or less than the posted range and this range may be modified in the future. No amount is considered to be wages or compensation until such amount is earned vested and determinable under the terms and conditions of the applicable policies and plans. The amount and availability of any bonus commission benefits or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole discretion unless and until paid and may be modified at the Companys sole discretion consistent with the law.
Statement
MacroGenics is proud to be an equal opportunity employer. Employment selection and related decisions are made without regard to race color national origin sex gender identity sexual orientation religion age disability protected veteran status or any other characteristic protected by federal state or local law. We are committed to working with and providing reasonable accommodation to individuals with disabilities. If because of a medical condition or disability you need a reasonable accommodation for any part of the employment process please email or call and/or 711 for TTD/TTY service.
Equal Opportunity Employer/Veterans/Disabled
We do notaccept non-solicited resumes or candidate submittals from search/recruiting agencies.
Required Experience:
IC
Summary of PositionThe Manufacturing Associate I participates in the manufacturing of biopharmaceutical drug product to support MacroGenics multiple clinical programs in the Cell Culture area. This position will work in the manufacturing suite under GMP (Good Manufacturing Practices) to ensure that ...
Summary of Position
The Manufacturing Associate I participates in the manufacturing of biopharmaceutical drug product to support MacroGenics multiple clinical programs in the Cell Culture area. This position will work in the manufacturing suite under GMP (Good Manufacturing Practices) to ensure that materials manufactured meet required specifications and regulatory requirements.
Responsibilities and Job Duties
- Participate in hands-on production in the manufacturing of material for clinical trials in a GMP environment including operating expansion and production reactors conducting harvest operations and ordering and accounting for consumption of raw materials and components.
- Contribute to the creation and revision of Batch Records Work Instructions Standard Operating Procedures Material Specifications and other GMP documents
- Adhere to all SOPs and execute batch records under GMP regulations documenting all manufacturing activities clearly and accurately including preparation records testing records equipment use records and laboratory notebooks
- Maintain adequate supplies and perform routine equipment maintenance
- Maintain manufacturing area in a clean neat and orderly condition at all times
- Participate in a variety of projects designed to improve the quality and efficiency of the manufacturing team
- Follow all related safety rules and procedures when working with hazardous materials
Qualifications
Education & Experience
- High School Diploma or equivalent with exposure to science and math coursework and a minimum of two years of related biopharmaceutical manufacturing experience in FDA regulated controlled production environment
OR
- Associates degree with one year of related biopharmaceutical manufacturing experience in FDA regulated controlled production environment
OR
- Bachelors degree in a related discipline with no experience
Knowledge Skills and Abilities
- Knowledge of cell culture techniques
- Ability to write and revise technical documents
- Ability to lift up to 30 lbs.
- Ability to work occasional weekends or overtime as needed
- Ability to follow detailed instructions and to maintain accurate records and notes
- Ability to work effectively in a team environment
- Ability to successfully perform multiple tasks when required
- Skills in problem solving and troubleshooting
- Ability to safely operate production equipment in accordance with established practices
Supervisory Responsibilities
None
Preferred Qualifications
- Previous GMP experience
- Ability to use MS Office (Word Excel)
Additional Information
The annual equivalent of pay for the Manufacturing Associate I position ranges from $47250 - $78750. For non-exempt roles and according to applicable regulations there may be the possibility for overtime pay. This role is eligible for the Companys discretionary bonus and discretionary equity incentives. Eligible employees may participate in the Companys benefits programs including medical / dental / vision / prescription coverage employee wellness resources 401(k) plan with employer match access to an Employee Stock Purchase Plan (ESPP) paid time off & paid parental leave benefits and disability benefits.
The annual pay rate range is described in good faith and the Company believes is the range of possible compensation for this role at the time of this posting depending on the candidates experience qualifications geographic location and other factors permitted by law. The Company may ultimately pay more or less than the posted range and this range may be modified in the future. No amount is considered to be wages or compensation until such amount is earned vested and determinable under the terms and conditions of the applicable policies and plans. The amount and availability of any bonus commission benefits or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole discretion unless and until paid and may be modified at the Companys sole discretion consistent with the law.
Statement
MacroGenics is proud to be an equal opportunity employer. Employment selection and related decisions are made without regard to race color national origin sex gender identity sexual orientation religion age disability protected veteran status or any other characteristic protected by federal state or local law. We are committed to working with and providing reasonable accommodation to individuals with disabilities. If because of a medical condition or disability you need a reasonable accommodation for any part of the employment process please email or call and/or 711 for TTD/TTY service.
Equal Opportunity Employer/Veterans/Disabled
We do notaccept non-solicited resumes or candidate submittals from search/recruiting agencies.
Required Experience:
IC
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