Cipla USA
Job Title : Quality Control (QC) Lab Technician
FLSA Classification : Full-Time, Non-Exempt/Hourly Professional
Work Location : Fall River, MA
Work Hours : Second Shift: 3:30 PM - 11:30 PM (may vary based on business needs)
Reports To : Quality Control Manager
Salary Range : $18.72 - 26.00/hr
Scope :
The scope is designed to describe the general nature and level of work as well as provide a basic understanding of the role, responsibilities, and expectations. This job description is not designed to provide an exact or exhaustive list of all job duties, tasks, skills, and qualifications. The intent is to give a general scope of the knowledge, skills, and abilities needed to satisfactorily perform the essential functions of the position and provide basic performance expectations. The scope of the job may be modified with respect to the department, group, and on an individual basis to a sometimes-specific testing group. Consideration of education, relevant training, and experience or a combination of all three may also result in further modification of the role.
Duties and Responsibilities
Perform sample management for all incoming raw materials, in-process, finished products and stability samples including receipt, logging, distribution and destruction.
Coordinate chemical and reference standard inventory in the lab, verifying the expired chemicals and standards and discarding as per company procedures.
Update all sample information in SAP as per company procedures.
Complete data entry as required.
Maintain lab consumables supply and place orders as needed.
Oversee temperature and humidity monitoring for stability chambers.
Conduct sample loading in stability chambers and submit stability samples as per schedule.
Assist in the shipment of samples to contract labs as required.
Provide general housekeeping in the QC lab and any other functional activity as assigned by management.
Other duties as assigned.
Education and Experience
Minimum of High School Diploma or equivalent (e.g., GED) required.
2 years’ work experience in a laboratory setting.
Proficient user of Microsoft Office Programs (Word, Excel, Outlook, PowerPoint) and other lab-related systems.
Associates degree or higher in Chemistry, Laboratory Science, or related fields preferred.
Bachelor’s degree (BS or BA) in physical sciences preferred.
Proficiently speak English as a first or second language.
Excellent organization, learning, and teaching skills required to work in teams.
Ability to understand and analyze complex data sets.
Experience in inhalation products (MDI) is a plus.
Professional and Behavioral Competencies
Hourly position.
Full time.
Must be willing to work in a pharmaceutical packaging setting.
Must be willing and able to work any assigned shift ranging from first or second shift.
Work schedule may be Monday to Friday.
Must be willing to work some weekends based on business needs as required by management.
Must possess a positive, professional attitude toward work and willingness to cooperate with co‑workers and supervisors.
No remote work available.
No employment sponsorship or work visas.
Working conditions This role works in a cGMP laboratory or manufacturing environment. Personal protective equipment is required, including uniforms, lab coats, safety glasses, respiratory protection, hearing protection, etc. Work with or around solvents, powders, or other materials commonly found in a pharmaceutical laboratory or manufacturing facility is required. The role may be assigned on a work‑shift basis (Day, Evening, Night). Weekend or holiday work may be requested or required. Long periods of standing/walking during the working hours; ability to ascend/descend ladders; and able to lift up to 35 pounds.
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FLSA Classification : Full-Time, Non-Exempt/Hourly Professional
Work Location : Fall River, MA
Work Hours : Second Shift: 3:30 PM - 11:30 PM (may vary based on business needs)
Reports To : Quality Control Manager
Salary Range : $18.72 - 26.00/hr
Scope :
The scope is designed to describe the general nature and level of work as well as provide a basic understanding of the role, responsibilities, and expectations. This job description is not designed to provide an exact or exhaustive list of all job duties, tasks, skills, and qualifications. The intent is to give a general scope of the knowledge, skills, and abilities needed to satisfactorily perform the essential functions of the position and provide basic performance expectations. The scope of the job may be modified with respect to the department, group, and on an individual basis to a sometimes-specific testing group. Consideration of education, relevant training, and experience or a combination of all three may also result in further modification of the role.
Duties and Responsibilities
Perform sample management for all incoming raw materials, in-process, finished products and stability samples including receipt, logging, distribution and destruction.
Coordinate chemical and reference standard inventory in the lab, verifying the expired chemicals and standards and discarding as per company procedures.
Update all sample information in SAP as per company procedures.
Complete data entry as required.
Maintain lab consumables supply and place orders as needed.
Oversee temperature and humidity monitoring for stability chambers.
Conduct sample loading in stability chambers and submit stability samples as per schedule.
Assist in the shipment of samples to contract labs as required.
Provide general housekeeping in the QC lab and any other functional activity as assigned by management.
Other duties as assigned.
Education and Experience
Minimum of High School Diploma or equivalent (e.g., GED) required.
2 years’ work experience in a laboratory setting.
Proficient user of Microsoft Office Programs (Word, Excel, Outlook, PowerPoint) and other lab-related systems.
Associates degree or higher in Chemistry, Laboratory Science, or related fields preferred.
Bachelor’s degree (BS or BA) in physical sciences preferred.
Proficiently speak English as a first or second language.
Excellent organization, learning, and teaching skills required to work in teams.
Ability to understand and analyze complex data sets.
Experience in inhalation products (MDI) is a plus.
Professional and Behavioral Competencies
Hourly position.
Full time.
Must be willing to work in a pharmaceutical packaging setting.
Must be willing and able to work any assigned shift ranging from first or second shift.
Work schedule may be Monday to Friday.
Must be willing to work some weekends based on business needs as required by management.
Must possess a positive, professional attitude toward work and willingness to cooperate with co‑workers and supervisors.
No remote work available.
No employment sponsorship or work visas.
Working conditions This role works in a cGMP laboratory or manufacturing environment. Personal protective equipment is required, including uniforms, lab coats, safety glasses, respiratory protection, hearing protection, etc. Work with or around solvents, powders, or other materials commonly found in a pharmaceutical laboratory or manufacturing facility is required. The role may be assigned on a work‑shift basis (Day, Evening, Night). Weekend or holiday work may be requested or required. Long periods of standing/walking during the working hours; ability to ascend/descend ladders; and able to lift up to 35 pounds.
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