Key Responsibilities
- Lead manufacturing projects to enhance process efficiency yield quality cycle time & cost reduction.
- Utilize statistical process control to monitor performance & develop plans to increase robustness & quality control.
- Provide technical support for manufacturing investigations & laboratory experiments.
- Conduct structured problem-solving investigations.
- Document process deviations & assess impact on quality & yield.
- Participate in cross functional teams by handling project management tasks.
- Lead process validation for technology transfers operational changes & new technologies.
- Support experimental & validation lot execution maintaining compliance with current procedures & regulations.
Provide technical support during regulatory audits & submissions & demonstrate accountability for EHS performance.
Qualifications :
Education & Experience
Must possess a BS in Chemistry Biology or Engineering (Chemical Mechanical Bio-chemical or other relevant scientific field) or equivalent education & 5 years of experience as a scientist in the pharmaceutical/medical device/chemical industry.
Of experience required must have 5 years:
- applying fundamentals of pharmaceutical drug product process including sterile/aseptic product manufacturing media fill sterilization fill finish operations & cGMP;
- performing design control process validation & technology transfer;
- providing regulatory support for IND and BLA submission;
- performing statistical analysis using Minitab JMP Lean Six Sigma);
- experience in project management working in a cross functional organization; &
- preparing scientific documents & reports orally & in writing for peers business stakeholders management & vendors.
Alternatively would accept MS or equivalent education Chemistry Biology or Engineering (Chemical Mechanical Bio-chemical or other relevant scientific field) & 1 year of experience as a scientist in the pharmaceutical/medical device/chemical industry.
Of experience required must have 1 year of each of (i) (ii) (iii) (iv) (v) (vi) & (vii).
Work experience may be gained concurrently. Will accept reasonable combination of education training & work experience.
Additional Information :
Salary Range: $115000.00 - $157500.00 per year.
Apply online at or send resume to . Refer to Req ID: REF49711S
We offer a comprehensive package of benefits including paid time off (vacation holidays sick) medical/dental/vision insurance and 401(k) to eligible employees. This job is eligible to participate in our short-term and long-term incentive programs.
AbbVie is committed to operating with integrity driving innovation transforming lives serving our community and embracing diversity and inclusion. It is AbbVies policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race color religion national origin age sex (including pregnancy) physical or mental disability medical condition genetic information gender identity or expression sexual orientation marital status status as a protected veteran or any other legally protected group status.
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
Work :
No
Employment Type :
Full-time
Key ResponsibilitiesLead manufacturing projects to enhance process efficiency yield quality cycle time & cost reduction.Utilize statistical process control to monitor performance & develop plans to increase robustness & quality control.Provide technical support for manufacturing investigations & lab...
Key Responsibilities
- Lead manufacturing projects to enhance process efficiency yield quality cycle time & cost reduction.
- Utilize statistical process control to monitor performance & develop plans to increase robustness & quality control.
- Provide technical support for manufacturing investigations & laboratory experiments.
- Conduct structured problem-solving investigations.
- Document process deviations & assess impact on quality & yield.
- Participate in cross functional teams by handling project management tasks.
- Lead process validation for technology transfers operational changes & new technologies.
- Support experimental & validation lot execution maintaining compliance with current procedures & regulations.
Provide technical support during regulatory audits & submissions & demonstrate accountability for EHS performance.
Qualifications :
Education & Experience
Must possess a BS in Chemistry Biology or Engineering (Chemical Mechanical Bio-chemical or other relevant scientific field) or equivalent education & 5 years of experience as a scientist in the pharmaceutical/medical device/chemical industry.
Of experience required must have 5 years:
- applying fundamentals of pharmaceutical drug product process including sterile/aseptic product manufacturing media fill sterilization fill finish operations & cGMP;
- performing design control process validation & technology transfer;
- providing regulatory support for IND and BLA submission;
- performing statistical analysis using Minitab JMP Lean Six Sigma);
- experience in project management working in a cross functional organization; &
- preparing scientific documents & reports orally & in writing for peers business stakeholders management & vendors.
Alternatively would accept MS or equivalent education Chemistry Biology or Engineering (Chemical Mechanical Bio-chemical or other relevant scientific field) & 1 year of experience as a scientist in the pharmaceutical/medical device/chemical industry.
Of experience required must have 1 year of each of (i) (ii) (iii) (iv) (v) (vi) & (vii).
Work experience may be gained concurrently. Will accept reasonable combination of education training & work experience.
Additional Information :
Salary Range: $115000.00 - $157500.00 per year.
Apply online at or send resume to . Refer to Req ID: REF49711S
We offer a comprehensive package of benefits including paid time off (vacation holidays sick) medical/dental/vision insurance and 401(k) to eligible employees. This job is eligible to participate in our short-term and long-term incentive programs.
AbbVie is committed to operating with integrity driving innovation transforming lives serving our community and embracing diversity and inclusion. It is AbbVies policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race color religion national origin age sex (including pregnancy) physical or mental disability medical condition genetic information gender identity or expression sexual orientation marital status status as a protected veteran or any other legally protected group status.
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
Work :
No
Employment Type :
Full-time
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