Senior Scientist

Lampire Biological Laboratories; Coopersburg (Lehigh County); On-site; USD 90,000 - 150,000; Full time

Job summary

Lampire Biological Labs, Inc. is seeking a qualified candidate to develop custom client processes and purifications within a production laboratory setting.

The role emphasizes coordination of processes, cGMP adherence, and collaboration with clients and internal teams. Required qualifications include a PhD or Master’s in a scientific field with experience, strong communication skills, and proficiency with Word/Excel.

Qualifications

• NOTE: Qualifications are based upon education, resume and/or work experience.
• Experience with cGMP quality systems and manufacturing operations.
• Good oral and written communications skills (English) and mathematical skills are required.
• Windows based computer skills, familiarity with Microsoft Word and Excel.
• A valid driver’s license in good standing for a minimum of 3 years.
• Good organizational skills with the ability to work independently or as a group, manage multiple priorities, and complete assigned tasks.

Responsibilities

• Formulate custom buffers based on client specifications or company needs and assist in preparation.
• Assist with custom purification of antibodies.
• Participate in client meetings as a subject matter expert.
• Utilize expertise to coordinate with clients in the establishment of custom purification methods based on the internal or external client needs or specifications.
• Assist in the research and development of products, procedures, and improvements to product quality.
• Assist laboratory staff as a subject matter expert.
• Write and revise Standard Operating Procedures (SOPs) and Batch Records (BR) as needed.
• Assist in filling, labeling and finished good inspection as needed.
• Operate laboratory and analytical equipment.
• Maintain cleanliness of workspace.
• Perform all work in accordance with good manufacturing practices (cGMP) and relevant SOP's.
• Assist in preparation of investigation reports as part of the Corrective and Preventative Action (CAPA) program.
• Other duties as assigned.

Skills

Communication skills

Mathematical skills

Windows skills

MS Word

MS Excel

Driver's license

Organizational skills

cGMP experience

Training others

Safety awareness

Lab equipment operation

Quality systems

Metric system

Education

PhD in a scientific field

Master's degree in a scientific field

Job description

Scope of Responsibility:

Responsible for the development of custom client processes and purifications and the coordination and communication of such processes within a production laboratory environment.

Supervisory Responsibilities:

None.

Position Requirements:

NOTE: Qualifications are based upon education, resume and/or work experience.

• Good oral and written communications skills (English) and mathematical skills are required.
• Windows based computer skills, familiarity with Microsoft Word and Excel.
• A valid driver’s license in good standing for a minimum of 3 years.
• Good organizational skills with the ability to work independently or as a group, manage multiple priorities, and complete assigned tasks.
• Experience with cGMP quality systems and manufacturing operations.
• Ability to give directions, train others, and communicate effectively.
• Thorough understanding of the metric system.
• Ability to perform all work (labor, tool use, equipment operation, etc.), and interact with others in a safe a responsible manner.

Essential Functions include (but are not limited to):

• Formulate custom buffers based on client specifications or company needs and assist in preparation.
• Assist with custom purification of antibodies.
• Participate in client meetings as a subject matter expert.
• Utilize expertise to coordinate with clients in the establishment of custom purification methods based on the internal or external client needs or specifications.
• Assist in the research and development of products, procedures, and improvements to product quality.
• Assist laboratory staff as a subject matter expert.
• Write and revise Standard Operating Procedures (SOPs) and Batch Records (BR) as needed.
• Assist in filling, labeling and finished good inspection as needed.
• Operate laboratory and analytical equipment.
• Maintain cleanliness of workspace.
• Perform all work in accordance with good manufacturing practices (cGMP) and relevant SOP's.
• Assist in preparation of investigation reports as part of the Corrective and Preventative Action (CAPA) program.
• Other duties as assigned.

Education:

• PhD in a scientific field preferred; or
• Master's degree in a scientific field with 3-5 years of related experience.

Physical Requirements:

• This position is moderately active and requires standing, walking, bending, and moving throughout the lab.
• The employee will need to be able to lift and/or move items up to 50 pounds.
• Must be able to access and navigate each department at the organization’s facilities.

Working Conditions:

• While performing the duties of this job, the employee is frequently standing, walking, and sitting.
• Conditions in the work environment are generally quiet, periodically there may be mid-level noise from various equipment.

Lampire Biological Labs, Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, or any other protected status under applicable law.