Lupin Pharmaceuticals (Company Headquarters)

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1 week ago(1/12/2018 11:37 AM)
Responsible for overseeing the progress of all pharmaceutics work with complex generic and brand products (which may include oral solids and liquids, thin films, topicals, and drug/device combination products) from early development to commercialization; will have responsibility for conducting product and process development activities in support of the company’s internal and collaborative drug development efforts. The candidate will be responsible for managing the pharmaceutics aspects and establish control strategies of our development programs. Currently all complex product development is conducted at third party contract facilities, and supporting these activities will require some travel. There is the potential that future development activities may (a) be brought back, in whole or in part, into a Lupin facility, and/or (b) be supported by the creation of an internal (to Lupin) pharmaceutical development laboratory.
ID
2018-2238
1 month ago(12/21/2017 5:03 PM)
The Pharmaceutical Manufacturing Investigations Specialist reports to the Manager of QA Investigations and is responsible for activities related to the investigations/deviations/CAPA process. Responsibilities include conducting the investigations, writing summary reports, suggesting and implementing appropriate corrective actions, and verifying effectiveness of CAPA. Additional responsibilities include administrative and compliance support to the Quality department within the Lupin Somerset facility. To be successful in this position a person must have a thorough understanding of the pharmaceutical manufacturing process including but not limited to Blending, Granulation, Encapsulation, and Compression. Above average writing and communication skills are imperative.
ID
2017-2230
1 month ago(12/21/2017 5:02 PM)
The QA Compliance Training Manager reports to the Associate Director of Site Compliance and is responsible for creating, implementing and monitoring training programs that include but are not limited to Competency Based Technical and cGMP (Current Good Manufacturing Practices). The Training Manager position is a hands-on position that requires daily support of the SABA LMS (Leaning Management System) Training Software and active participation in development and delivery of SOP’s, Ethics and Code of Conduct, EHS, and ongoing cGMP training.  This position supports site audits and site metrics preparation and assessment.  Effective business partnering to assess individual departments’ training needs is essential.            
ID
2017-2229
1 month ago(12/11/2017 12:04 PM)
The position is responsible for operating liquid filling equipment including trouble shooting and making minor mechanical adjustments. Must be able to keep accurate and detailed records, understand batch records and maintain cleanliness of work area.  Must follow standard operating procedures for the packaging operation.  First shift hours are 6am to 2:30pm.              
ID
2017-2226
2 months ago(12/1/2017 10:35 AM)
  The Warehouse Associate is responsible for organization of inventory in the warehouse, as well as tracking and facilitation of shipping and receiving.  The Associate will be working with pharmaceutical ingredients and is expected to adhere to strict GMP guidelines. Maintaining a safe work environment is imperative.    
ID
2017-2224
3 months ago(11/2/2017 3:44 PM)
The position entails operating compression equipment including trouble shooting and minor mechanical adjustments. Must be able to keep accurate and detailed records, understand the batch records, and maintain cleanliness of work area. Follow standard operating procedures for the production operation.  Second shift hours are 3pm to 12am.
ID
2017-2199
3 months ago(10/31/2017 3:55 PM)
The position is responsible for operating pharmaceutical packaging equipment including trouble shooting and making minor mechanical adjustments.  Must be able to keep accurate and detailed records, understand batch records and maintain cleanliness of work area.  Must follow standard operating procedures for the packaging operation. 
ID
2017-2194
3 months ago(10/5/2017 3:06 PM)
Perform testing and decide on the acceptability of the in-process, process validation samples, finished products, stability samples and developmental samples in a regulated laboratory environment. Analyze and interpret results in written and oral format.
ID
2017-2159
6 months ago(7/6/2017 11:18 AM)
Perform testing and decide on the acceptability of the in-process, process validation samples, finished products, stability samples and developmental samples in a regulated laboratory environment. Analyze and interpret results in written and oral format.
ID
2017-2133
3 months ago(11/1/2017 2:49 PM)
The position entails operating blending equipment including trouble shooting and minor mechanical adjustments. Must be able to keep accurate and detailed records, understand the batch records, and maintain cleanliness of work area. Follow standard operating procedures for the production operation.  Second shift hours are 3:30pm to 12:00am.
ID
2017-2125
4 months ago(10/3/2017 2:04 PM)
The Sr. Validation Scientist/Engineer is responsible for carrying out validation activities as they relate to manufacturing and packaging processes, process hold times, cleaning processes, and facilities/utilities/equipment within the Lupin Somerset site. This position assures that all validation activities are executed with the highest quality and meet all applicable SOP’s and regulatory standards. This position will also be responsible for leading Validation projects.
ID
2017-2057
4 months ago(9/27/2017 10:58 AM)
The Quality Assurance Technician I is responsible for the assurance of proper GMP activities within the Lupin Somerset manufacturing and packaging facilities. This position is responsible for working in production, warehouse, process rooms and packaging lines to evaluate all manufacturing activities meet the acceptance criteria. Second shift is 3:30pm to 12:00am.
ID
2017-2056