AbbVie's Biologics Drug Product Development (Bio DPD) within Development Sciences is a global organization responsible for drug product formulation and process development, and definition of product ...
AbbVie's Biologics Drug Product Development (Bio DPD) within Development Sciences is a global organization responsible for drug product formulation and process development, and definition of product ...
## Associate Director, Technical Operations (Analytical Development-Biologics)Applylocations: San ... Oversee specification setting of drug substance and drug product at CDMOs/CROs.* Author/review ...
## Associate Director, Technical Operations (Analytical Development-Biologics)Applylocations: San ... Oversee specification setting of drug substance and drug product at CDMOs/CROs.* Author/review ...
Position Overview The Associate Director, Drug Substance MSAT, leads end-to-end process stewardship ... product, including process development and Good Manufacturing Practices (GMP) Preferred ...
Position Overview The Associate Director, Drug Substance MSAT, leads end-to-end process stewardship ... product, including process development and Good Manufacturing Practices (GMP) Preferred ...
Position Overview The Associate Director, Drug Substance MSAT, leads end-to-end process stewardship ... product, including process development and Good Manufacturing Practices (GMP) Preferred ...
Position Overview The Associate Director, Drug Substance MSAT, leads end-to-end process stewardship ... product, including process development and Good Manufacturing Practices (GMP) Preferred ...
Associate Director/Principal Scientist, CMC Analytical Chemistry Location: San Francisco, CA or ... development, validation and implementation of QC methods for drug substance, drug product ...
Quick apply
Associate Director/Principal Scientist, CMC Analytical Chemistry Location: San Francisco, CA or ... development, validation and implementation of QC methods for drug substance, drug product ...
Associate Director/Principal Scientist, CMC Analytical Chemistry
San Francisco, CA Β· On-site
$190K - $220K/yr
Associate Director/Principal Scientist, CMC Analytical Chemistry Location: San Francisco, CA or ... development, validation and implementation of QC methods for drug substance, drug product ...
Associate Director/Principal Scientist, CMC Analytical Chemistry
San Francisco, CA Β· On-site
$190K - $220K/yr
Associate Director/Principal Scientist, CMC Analytical Chemistry Location: San Francisco, CA or ... development, validation and implementation of QC methods for drug substance, drug product ...
Senior Advisor, Drug Product - CMC
Boston, MA Β· On-site
$140K - $195K/yr
Operating at the Associate Director level, the successful candidate will have a demonstrated track ... Support clinical formulation development of oral solid dosage forms, as needed. * Author and/or ...
Senior Advisor, Drug Product - CMC
Boston, MA Β· On-site
$140K - $195K/yr
Operating at the Associate Director level, the successful candidate will have a demonstrated track ... Support clinical formulation development of oral solid dosage forms, as needed. * Author and/or ...
Lead drug product (DP) process development activities across different unit operations for multiple programs. * Support implementation of cross-scale models to bridge lab and manufacturing for an ...
Lead drug product (DP) process development activities across different unit operations for multiple programs. * Support implementation of cross-scale models to bridge lab and manufacturing for an ...
Assoc Director, Pharmaceutical Development
South San Francisco, CA Β· On-site
$190K - $210K/yr
Reporting to the Sr Director of Pharmaceutical Development, the Associate Director of ... Manage day-to-day clinical drug product manufacturing activities at CDMOs to ensure timely delivery.
Quick apply
Assoc Director, Pharmaceutical Development
South San Francisco, CA Β· On-site
$190K - $210K/yr
Reporting to the Sr Director of Pharmaceutical Development, the Associate Director of ... Manage day-to-day clinical drug product manufacturing activities at CDMOs to ensure timely delivery.
Job Summary The Senior Director - Executive Medical Director, Drug Development is responsible for ... Provide guidance for successful implementation of investigator-initiated trials for product ...
Job Summary The Senior Director - Executive Medical Director, Drug Development is responsible for ... Provide guidance for successful implementation of investigator-initiated trials for product ...
Scientist II, Drug Product
Redwood City, CA Β· On-site
Contribute to drug product development activities for new chemical entities (NCEs) from early development through late-stage clinical development, with exposure to commercialization activities.
Scientist II, Drug Product
Redwood City, CA Β· On-site
Contribute to drug product development activities for new chemical entities (NCEs) from early development through late-stage clinical development, with exposure to commercialization activities.
Oncology drug development and precision medicine expertise; experience with targeted/bio ... marketed products. Benefits * Eligible for annual bonus and equity incentive awards (not ...
Oncology drug development and precision medicine expertise; experience with targeted/bio ... marketed products. Benefits * Eligible for annual bonus and equity incentive awards (not ...
SUMMARY BioMarin is seeking an experienced and motivated Associate Director to join our Combination ... Experience with lyophilized product related drug delivery EDUCATION Bachelor's degree in ...
SUMMARY BioMarin is seeking an experienced and motivated Associate Director to join our Combination ... Experience with lyophilized product related drug delivery EDUCATION Bachelor's degree in ...
Biologics Drug Product Development (Bio DPD), a part of Development Sciences within AbbVie's R&D, is a global organization that is responsible for drug product formulation and process development ...
Biologics Drug Product Development (Bio DPD), a part of Development Sciences within AbbVie's R&D, is a global organization that is responsible for drug product formulation and process development ...
The Associate Director, Drug Substance MSAT, leads end-to-end process stewardship (Upstream and ... product, including process development and Good Manufacturing Practices (GMP) Preferred ...
The Associate Director, Drug Substance MSAT, leads end-to-end process stewardship (Upstream and ... product, including process development and Good Manufacturing Practices (GMP) Preferred ...
Direct industry experience in biologics drug product development. Required Experience and Skills: * Hands-on experience in formulation development for recombinant proteins, including antibodies, ADCs ...
Direct industry experience in biologics drug product development. Required Experience and Skills: * Hands-on experience in formulation development for recombinant proteins, including antibodies, ADCs ...
Associate Director - Technical Services/Manufacturing Science - Bioconjugate/Drug Product
Richmond, VA Β· On-site
The Associate Director - TS/MS - Bioconjugate/Drug Product Manufacturing, will lead a technical ... Support the development and implementation of robust control strategies to ensure regulatory ...
Associate Director - Technical Services/Manufacturing Science - Bioconjugate/Drug Product
Richmond, VA Β· On-site
The Associate Director - TS/MS - Bioconjugate/Drug Product Manufacturing, will lead a technical ... Support the development and implementation of robust control strategies to ensure regulatory ...
Associate Director - Technical Services/Manufacturing Science - Bioconjugate/Drug Product
Richmond, VA Β· On-site
The Associate Director - TS/MS - Bioconjugate/Drug Product Manufacturing, will lead a technical ... Support the development and implementation of robust control strategies to ensure regulatory ...
Associate Director - Technical Services/Manufacturing Science - Bioconjugate/Drug Product
Richmond, VA Β· On-site
The Associate Director - TS/MS - Bioconjugate/Drug Product Manufacturing, will lead a technical ... Support the development and implementation of robust control strategies to ensure regulatory ...
Process Development Senior Scientist - Pre-Pivotal Drug Product Technologies
Thousand Oaks, CA Β· On-site
Proven experience in formulation development, stability testing, and fill/finish operations for biologics; direct biologics drug product formulation experience is strongly preferred. * Demonstrated ...
Process Development Senior Scientist - Pre-Pivotal Drug Product Technologies
Thousand Oaks, CA Β· On-site
Proven experience in formulation development, stability testing, and fill/finish operations for biologics; direct biologics drug product formulation experience is strongly preferred. * Demonstrated ...
Associate Director, CMC - Analytical Development
Boston, MA Β· On-site
$170K - $220K/yr
In addition, the Associate Director provides analytical expertise to the Sr. Director of Precursor ... and drug products, to support product development and regulatory objectives. * Partner with ...
Associate Director, CMC - Analytical Development
Boston, MA Β· On-site
$170K - $220K/yr
In addition, the Associate Director provides analytical expertise to the Sr. Director of Precursor ... and drug products, to support product development and regulatory objectives. * Partner with ...
Associate Director Drug Product Development information
See salary details
$21K - $35.5K
1% of jobs
$35.5K - $49.9K
3% of jobs
$49.9K - $64.4K
12% of jobs
$71.2K is the 25th percentile. Wages below this are outliers.
$64.4K - $78.8K
19% of jobs
The median wage is $85K / yr.
$78.8K - $93.3K
35% of jobs
$98.7K is the 75th percentile. Wages above this are outliers.
$93.3K - $107.7K
13% of jobs
$107.7K - $122.2K
6% of jobs
$122.2K - $136.6K
4% of jobs
$136.6K - $151.1K
3% of jobs
$151.1K - $165.5K
1% of jobs
$165.5K - $180K
2% of jobs
$21K
$93.3K
$180K
How much do associate director drug product development jobs pay per year?
What are popular job titles related to Associate Director Drug Product Development jobs?
For Associate Director Drug Product Development jobs, the most frequently searched job titles are:

Senior Scientist II, Biologics Drug Product Development
North Chicago, IL β’ On-site
Other
Medical, Dental, Vision, Retirement, PTO
Posted 25 days ago
Key responsibilities
Lead matrix drug product teams for internal and external projects and represent Bio DPD in crossβfunctional teams.
Design and execute biologics drug product formulation development, characterization, and robustness studies.
Communicate development plans, risks, and mitigation strategies to stakeholders and line management.
Job description
AbbVie's Biologics Drug Product Development (Bio DPD) within Development Sciences is a global organization responsible for drug product formulation and process development, and definition of product presentation for biologics (proteins, conjugates, peptides, neurotoxins, etc.) and genetic medicine (AAV, LNPs, Cell Therapy). AbbVie seeks a highly motivated Senior Scientist II located in North Chicago, IL, with a proven track record in biologics drug product formulation development, predictive stability, inβuse, and quality risk management.
Key Responsibilities- Lead matrix drug product teams for one or more internal and external projects and represent Bio DPD in the crossβfunctional Product Presentation and Device Strategy Team (PPDST) and the CMC Team.
- Lead the design and execution of biologics drug product formulation development, characterization and robustness studies.
- Serve as subject matter expert in biologics predictive stability modeling, inβuse and administration procedures, and QRM.
- Effectively and timely communicate development plans, risks, and mitigation plans to stakeholders and line management.
- Initiate and/or support scientific initiatives to drive innovation, continuously enhance capabilities and platforms, and improve business processes.
- Bachelorβs, Masterβs, or PhD in Pharmaceutics, Pharmaceutical Sciences, Chemistry, Chemical Engineering, or related disciplines with 12+ years (Bachelors), 10+ years (Masters), or 4+ years (PhD) of relevant industry experience.
- Proven ability to solve critical scientific problems.
- Experience leading drug product development as the functional lead within crossβfunctional teams.
- Strong experience with biologics (proteins, conjugates, peptides and/or neurotoxins) and/or genetic medicine (AAV, LNPs, cell therapy) formulation development, and QRM.
- Strong experience in predictive stability modeling (statistical, phenomenological, mechanistic, and/or AI/ML) for biologics.
- Strong experience in inβuse compatibility and stability for biologics products.
- Strong experience in quality risk management.
- Understanding of relevant cGMP and regulatory guidance.
- Experience with sterile manufacturing unit operations (freezeβthaw, compounding, mixing, filtration and filling) development, characterization, scaleβup and technology transfer.
- Experience managing thirdβparty manufacturers of sterile parenteral products.
- Experience with quality risk management and drug product control strategies.
- Deep scientific knowledge and significant handsβon experience with predictive stability modeling, administration procedures and risk management.
- Effectively communicates to influence without authority, drives technical excellence, and inspires continuous improvement.
- Builds strong relationships with peers and crossβfunctional partners to enable higher performance.
- Connects ideas from disparate fields, integrates data and information quickly, and takes risks to achieve the highest performance.
- Raises the bar and is never satisfied with the status quo.
- Creates a learning environment, open to suggestions and experimentation for improvement.
- Embraces the ideas of others, nurtures innovation and manages innovation to reality.
The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and may ultimately pay more or less than the posted range. This range may be modified in the future.
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 longβterm incentive programs.
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.