What are the responsibilities and job description for the Associate Scientist position at Hikma Pharmaceuticals?
Job Title: Associate Scientist
Location: Cherry Hill, New Jersey
Job Type Fulltime
Description:
We continue to be committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds. We are seeking a talented and motivated Process Supervisor. In this role, you will be responsible for managing shift or multiple shift operations within manufacturing departments. Responsible for meeting budget, quality, and production goals, setting standards, and making employment and staffing decisions. Interprets manufacturing policies, procedures, and programs
Summary:
This position supports the parenteral pharmaceutical manufacturing facility through the qualification and/or validation of equipment, raw materials, and manufacturing processes. Validation activities include research, protocol writing/execution and final report generation. Additionally, investigations of manufacturing challenges are conducted, and process improvements are evaluated/implemented. Final documents are archived and may be included in or support A/NDA submissions and made available as needed during FDA, MHRA, and client/customer compliance audits.
Essential Duties and Responsibilities:
Under moderate oversight by senior team member or manager:
Education and/or Experience
Base Salary: $48,250.00 -$80,4000.00 annually. The compensation for this position will be determined during the interview process and will vary based on multiple factors, including, but not limited to, work location, prior experience and job-related knowledge, relevant skills and expertise, current business needs, and market factors. The Talent Acquisition team can provide more details about the specific salary range for the job location during the hiring process.
Equal Opportunity Employer:
Hikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law.
Location: Cherry Hill, New Jersey
Job Type Fulltime
Description:
We continue to be committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds. We are seeking a talented and motivated Process Supervisor. In this role, you will be responsible for managing shift or multiple shift operations within manufacturing departments. Responsible for meeting budget, quality, and production goals, setting standards, and making employment and staffing decisions. Interprets manufacturing policies, procedures, and programs
Summary:
This position supports the parenteral pharmaceutical manufacturing facility through the qualification and/or validation of equipment, raw materials, and manufacturing processes. Validation activities include research, protocol writing/execution and final report generation. Additionally, investigations of manufacturing challenges are conducted, and process improvements are evaluated/implemented. Final documents are archived and may be included in or support A/NDA submissions and made available as needed during FDA, MHRA, and client/customer compliance audits.
Essential Duties and Responsibilities:
Under moderate oversight by senior team member or manager:
- Applies knowledge or quickly learns cGMPs, relevant SOP curriculum, routine project procedures, project management, and other training as appropriate.
- Performs a variety of projects/studies in areas that may include Product/Process, Sterilization, Cleaning and Equipment Validation, as well as Projects/Studies to support Manufacturing Operations.
- Writes protocols, reports (GTRs), Change Controls (including MARs). Conducts Studies/Executes protocols.
- Serves as project lead with projects of intermediate scope and cross-functional teams.
- Handles routine tasks timely, accurately.
- Ability to communicate effectively at all levels in verbal and written form, including technical/business writing.
- Proficient in Microsoft Word and Excel, computer software.
- Direct industry knowledge.
- Ability to work independently or in teams.
- Ability to walk some distance 1 to 3 miles, stand for 3 to 6 hours and lift 10 to 40 lbs. during the course of a work day as required.
- Ability to work any shift (1st, 2nd or 3rd) on any day of the week (7 days) as duties require.
- Ability to become clean room gown trained/qualified and to work within the sterile suite areas for up to a full 8-hour shift (with appropriate breaks).
Education and/or Experience
- Minimum of a BA or BS preferably in the Sciences/Engineering/Math (other degrees accepted provided the individual has relevant experience -- e.g. education or employment in sciences or validations).
Base Salary: $48,250.00 -$80,4000.00 annually. The compensation for this position will be determined during the interview process and will vary based on multiple factors, including, but not limited to, work location, prior experience and job-related knowledge, relevant skills and expertise, current business needs, and market factors. The Talent Acquisition team can provide more details about the specific salary range for the job location during the hiring process.
Equal Opportunity Employer:
Hikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law.
Salary : $48,250 - $804,000