Charleston, SC · On-site
$99K - $128K/yr
... pharmaceutical manufacturing environment. * Previous experience supporting tech transfer of ... Working knowledge of cGMP requirements related to sterile Drug Product manufacturing processes.
Charleston, SC · On-site
$99K - $128K/yr
... pharmaceutical manufacturing environment. * Previous experience supporting tech transfer of ... Working knowledge of cGMP requirements related to sterile Drug Product manufacturing processes.
Charleston, SC · On-site
$99K - $128K/yr
... pharmaceutical manufacturing environment. * Previous experience supporting tech transfer of ... Working knowledge of cGMP requirements related to sterile Drug Product manufacturing processes.
Charleston, SC · On-site
$99K - $128K/yr
... pharmaceutical manufacturing environment. * Previous experience supporting tech transfer of ... Working knowledge of cGMP requirements related to sterile Drug Product manufacturing processes.
Clinton, TN · On-site
Process Engineer ???? Clinton, TN | Full-time ???? Vacancies: 1 About Tjoapack Tjoapack is a global ... At least one year of working in a Pharmaceutical cGMP evironment is required for consideration.
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Clinton, TN · On-site
Process Engineer ???? Clinton, TN | Full-time ???? Vacancies: 1 About Tjoapack Tjoapack is a global ... At least one year of working in a Pharmaceutical cGMP evironment is required for consideration.
New Brunswick, NJ · On-site
Company Description Big Pharmaceutical Organisation Associate Process Engineer/Scientist- Drug ... Working competency of Statistical Process Control and related tools (JMP/MiniTab/SAS). Able to ...
New Brunswick, NJ · On-site
Company Description Big Pharmaceutical Organisation Associate Process Engineer/Scientist- Drug ... Working competency of Statistical Process Control and related tools (JMP/MiniTab/SAS). Able to ...
Concord, NC · On-site
Required Qualifications * 5+ years of experience in Process Validation within the pharmaceutical industry. * Experience working in a sterile manufacturing environment. * Strong experience with ...
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Concord, NC · On-site
Required Qualifications * 5+ years of experience in Process Validation within the pharmaceutical industry. * Experience working in a sterile manufacturing environment. * Strong experience with ...
Prepare processing rooms and equipment for R&D, pilot-scale and GMP manufacturing operations ... Experience working in a cGMP environment is desirable. * Knowledge of GMPs and other commonly used ...
Prepare processing rooms and equipment for R&D, pilot-scale and GMP manufacturing operations ... Experience working in a cGMP environment is desirable. * Knowledge of GMPs and other commonly used ...
North Charleston, SC · On-site
$99K - $128K/yr
... pharmaceutical manufacturing environment. * Previous experience supporting tech transfer of ... Working knowledge of cGMP requirements related to sterile Drug Product manufacturing processes.
North Charleston, SC · On-site
$99K - $128K/yr
... pharmaceutical manufacturing environment. * Previous experience supporting tech transfer of ... Working knowledge of cGMP requirements related to sterile Drug Product manufacturing processes.
Albany, GA · On-site
$90K - $95K/hr
Process Technology Specialist Industry: Medical Device / Pharmaceutical Manufacturing Job Type ... or pharmaceutical manufacturing * Experience working within an FDA-regulated and/or EU MDR ...
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Albany, GA · On-site
$90K - $95K/hr
Process Technology Specialist Industry: Medical Device / Pharmaceutical Manufacturing Job Type ... or pharmaceutical manufacturing * Experience working within an FDA-regulated and/or EU MDR ...
Responsible for managing the RDT structure and oversees the Roster Management process ... Experience working with field sales as well as IT preferred.
Responsible for managing the RDT structure and oversees the Roster Management process ... Experience working with field sales as well as IT preferred.
$99K - $128K/yr
... pharmaceutical manufacturing environment. * Previous experience supporting tech transfer of ... Working knowledge of cGMP requirements related to sterile Drug Product manufacturing processes.
$99K - $128K/yr
... pharmaceutical manufacturing environment. * Previous experience supporting tech transfer of ... Working knowledge of cGMP requirements related to sterile Drug Product manufacturing processes.
Responsible for managing the RDT structure and oversees the Roster Management process ... Experience working with field sales as well as IT preferred.
Responsible for managing the RDT structure and oversees the Roster Management process ... Experience working with field sales as well as IT preferred.
Responsible for managing the RDT structure and oversees the Roster Management process ... Experience working with field sales as well as IT preferred.
Quick apply
Responsible for managing the RDT structure and oversees the Roster Management process ... Experience working with field sales as well as IT preferred.
Charleston, SC · On-site
$97K - $125K/yr
... pharmaceutical manufacturing environment. * Previous experience supporting tech transfer of ... Working knowledge of cGMP requirements related to sterile Drug Product manufacturing processes.
Charleston, SC · On-site
$97K - $125K/yr
... pharmaceutical manufacturing environment. * Previous experience supporting tech transfer of ... Working knowledge of cGMP requirements related to sterile Drug Product manufacturing processes.
Indianapolis, IN · On-site
$99K - $128K/yr
Drive process improvements across pharmaceutical manufacturing operations. * Optimize fill line and ... Experience working with isolators and associated support systems. * Familiarity with autoclave and ...
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Indianapolis, IN · On-site
$99K - $128K/yr
Drive process improvements across pharmaceutical manufacturing operations. * Optimize fill line and ... Experience working with isolators and associated support systems. * Familiarity with autoclave and ...
Brighton, MI · On-site
$100K - $120K/yr
The Role Reporting to the Director, Pharmaceutical Technologies , the Manager, Process Development ... Promote a safe working environment and reinforce Biovire's commitment to quality, compliance, and ...
Brighton, MI · On-site
$100K - $120K/yr
The Role Reporting to the Director, Pharmaceutical Technologies , the Manager, Process Development ... Promote a safe working environment and reinforce Biovire's commitment to quality, compliance, and ...
Brighton, MI · On-site
$100K - $120K/yr
The RoleReporting to the Director, Pharmaceutical Technologies, the Manager, Process Development ... Promote a safe working environment and reinforce Biovire's commitment to quality, compliance, and ...
Quick apply
Brighton, MI · On-site
$100K - $120K/yr
The RoleReporting to the Director, Pharmaceutical Technologies, the Manager, Process Development ... Promote a safe working environment and reinforce Biovire's commitment to quality, compliance, and ...
Brighton, MI · On-site
The Role Reporting to the Director, Pharmaceutical Technologies , the Manager, Process Development ... Promote a safe working environment and reinforce Biovire's commitment to quality, compliance, and ...
Brighton, MI · On-site
The Role Reporting to the Director, Pharmaceutical Technologies , the Manager, Process Development ... Promote a safe working environment and reinforce Biovire's commitment to quality, compliance, and ...
... Process Equipment is responsible for driving compliant results in a GMP pharmaceutical ... while working closely with Engineering and other support teams. · Partner with engineering ...
... Process Equipment is responsible for driving compliant results in a GMP pharmaceutical ... while working closely with Engineering and other support teams. · Partner with engineering ...
... Process Equipment is responsible for driving compliant results in a GMP pharmaceutical ... while working closely with Engineering and other support teams. · Partner with engineering ...
... Process Equipment is responsible for driving compliant results in a GMP pharmaceutical ... while working closely with Engineering and other support teams. · Partner with engineering ...
... Process Equipment is responsible for driving compliant results in a GMP pharmaceutical ... while working closely with Engineering and other support teams. · Partner with engineering ...
... Process Equipment is responsible for driving compliant results in a GMP pharmaceutical ... while working closely with Engineering and other support teams. · Partner with engineering ...
For Process Worker Pharmaceutical jobs, the most frequently searched job titles are:
Charleston, SC • On-site
$99K - $128K/yr
Full-time
Re-posted 2 days ago
7.8
Based on 9 frontline employees who took The Breakroom Quiz
At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record.
Are you interested in joining our team?
The Sr. Process Engineer is accountable for driving results in a fast-paced environment by providing technical support for clinical and commercial parenteral Drug Product manufacturing. The Sr. Process Engineer’s responsibilities include but are not limited to the following: performing tech transfers of new processes and technologies into the site, preparation of documentation to support process validation and batch manufacturing, troubleshooting manufacturing processes, completing process deviations and investigations, and coordinating lab studies with the formulation development lab. These functions will be executed following standard operating procedures and batch records in accordance with FDA and EU requirements and current Good Manufacturing Practices.
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is required to frequently stand, walk, sit; talk or hear; use hands to finger, handle or feel. The employee is required some of the time to reach with hands and arms. The employee is required occasionally to climb or balance; and taste or smell. The employee must frequently lift and/or move up to 25 pounds. There is no special vision requirement for this job. The employee may occasionally work near moving mechanical parts; fumes or airborne particles; toxic or caustic chemicals.
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Pharmaceutical and medicine manufacturing
501 - 1,000 Employees
Durham, NC, US
1979
