JobMonkey, Inc.
Life Technologies (Thermo Fisher Scientific). Ohio, Cincinnati
JobMonkey, Inc., Cincinnati, Ohio, United States, 45208
Work Schedule
Standard (Mon-Fri)
Environmental Conditions Office, some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs, etc.)
Job Description As a Manufacturing Scientist II, you will lead and/or implement activities for the development of new and established wouldn't. Project management skills will be applied to implement the scaling up manufacturing processes, supporting new product validations and post‑approval qualification activities. This will require writing, approving, and routing documents within a manufacturing setting.
You will be the primary technical representative on client projects and will work closely with internal and external teams of analytical, quality, and project management representatives. Supporting process development and commercial activities will be required. Leads technical/scientific project activities and discussions to develop strategies and solutions that meet client needs and expectations.
Investigates, creates, and validates new scientific and equipment methodologies for a diverse range of projects. Uses experimental design, established formulation processes for the following phases of product scale‑up, registration, and validation.
Creates processes and equipment designs for clinical, scale‑up, and/or registration batches, including technology transfer of projects to and from clients. Leads problem tuyệtaaradda as necessary with independent judgement, making decisions that involve multiple options or develop new solutions to resolve moderately complex problems.
Time‑bound outlines to complete activities for the validation of new products and manufacturing processes of solids, liquids, and semi‑solid dosage forms.
Leverage current leadership skills to provide support, mentoring, and guidance to internal team members and clients for product and process development activities performed in commercial manufacturing areas.
Lead client calls as primary technical representative and provide scientific justification for the project decisions and recommendations.
Own the为什么 review and planning of all technical aspects of the project, which includes prioritization of multiple projects or tasks to meet the appropriate timeline achievements.
Integrate a risk‑based approach during the scale‑up and commercialization of processes ylabel and develop appropriate mitigation strategies.
Draft quality batch production records, protocols, and reports to support product development, validation activities, and routine commercial batches.
Support routine manufacturing operations to assure timely release of products with appropriate quality attributes and steward commercial products of responsibility.
Lead with project leadership skills required for daily meetings.
Work independently within the Technical Services Department and as a team member within the department.
Managing work independently with standard work planning and abilities to meet timelines established for projects.
Proficiencies in Leadership, Trust, Diversity, and Focused behaviors are required for the position.
Quality attitude to be exemplified daily with standard work.
Outstanding team dynamics and idea generation are promoted.
How will you get here? Education Bachelor's degree in chemical engineering (or other engineering field), chemistry, pharmacy, or another related science or technical field is required.
Experience
Minimum of one (1) to three (3) years of experience in a manufacturing environment preferred.
Experience in product or process development, including scale‑up and technology transfer processes for both immediate and controlled release dosage forms preferred.
Project Management experience preferred.
Knowledge, Skills, Abilities
Understanding of Good Manufacturing Practices (GMP) and regulatory compliance.
Lead projects of moderate to high complexity in scope and compliance‑related challenges to implement processes that meet changing regulations.
Proficiency using Microsoft (MS) Office applications.
Good critical and logical thinking skills. Effective written, interpersonal, and presentation skills, including leading technical discussions with internal and external clients.
Self‑starter, mature, independent, and detail oriented.
Ability to work in a fast‑paced, results‑oriented, and structured environment.
Experience leading projects related to process development, including scale‑up production activities.
Effective time management, multi‑tasking, and tracing skills to run multiple projects.
Lead by example.
Courages and assumes challenges in a risk‑based approach.
Transparent and knowledgeable in presenting project updates daily.
Diligent in team meetings and discussions.
Collaborate across multiple departments to reach goals and objectives.
Inclusive communication styles and ideas.
Conscientious toward fellow peers and work‑load requirements.
Coordinate and lead weekly meetings with customers.
Fast and focused execution of tasks will be required at times.
Build helpful ideas to increase production efficiencies.
Transfer technical skill information to supporting departments.n Participate and support audit participation and interaction for regulatory agencies.
Develop and transform learning for peers with technical and mechanical result‑oriented aptitudes.
Written communication skills expected, and presentation will be expected.
Equivalent combinations of education, training, and meaningful work experience may be considered.
Physical Requirements Position requires ordinary ambulatory skills and physical coordination sufficient to move around office and manufacturing locations; ability to stand, walk, stoop, kneel, crouch periodically, and manipulate light to medium weights (10–35 pounds). Requires arm, hand, and finger dexterity, including the ability to type for periods of time; visual acuity to use a keyboard, computer monitor, operate equipment, and read materials; ability to sit, reach with hands and arms, talk, and hear for prolonged periods.
zny- The Thermo Fisher team of 100,000 outstanding minds invites you to join and help enable our customers to make the world healthier, cleaner, and safer.
Apply today:
http://jobs.thermofisher.com
Thermo Fisher Scientific is an EEO Spielautomaten and affirmative action employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status.
#J-18808-Ljbffr
Environmental Conditions Office, some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs, etc.)
Job Description As a Manufacturing Scientist II, you will lead and/or implement activities for the development of new and established wouldn't. Project management skills will be applied to implement the scaling up manufacturing processes, supporting new product validations and post‑approval qualification activities. This will require writing, approving, and routing documents within a manufacturing setting.
You will be the primary technical representative on client projects and will work closely with internal and external teams of analytical, quality, and project management representatives. Supporting process development and commercial activities will be required. Leads technical/scientific project activities and discussions to develop strategies and solutions that meet client needs and expectations.
Investigates, creates, and validates new scientific and equipment methodologies for a diverse range of projects. Uses experimental design, established formulation processes for the following phases of product scale‑up, registration, and validation.
Creates processes and equipment designs for clinical, scale‑up, and/or registration batches, including technology transfer of projects to and from clients. Leads problem tuyệtaaradda as necessary with independent judgement, making decisions that involve multiple options or develop new solutions to resolve moderately complex problems.
Time‑bound outlines to complete activities for the validation of new products and manufacturing processes of solids, liquids, and semi‑solid dosage forms.
Leverage current leadership skills to provide support, mentoring, and guidance to internal team members and clients for product and process development activities performed in commercial manufacturing areas.
Lead client calls as primary technical representative and provide scientific justification for the project decisions and recommendations.
Own the为什么 review and planning of all technical aspects of the project, which includes prioritization of multiple projects or tasks to meet the appropriate timeline achievements.
Integrate a risk‑based approach during the scale‑up and commercialization of processes ylabel and develop appropriate mitigation strategies.
Draft quality batch production records, protocols, and reports to support product development, validation activities, and routine commercial batches.
Support routine manufacturing operations to assure timely release of products with appropriate quality attributes and steward commercial products of responsibility.
Lead with project leadership skills required for daily meetings.
Work independently within the Technical Services Department and as a team member within the department.
Managing work independently with standard work planning and abilities to meet timelines established for projects.
Proficiencies in Leadership, Trust, Diversity, and Focused behaviors are required for the position.
Quality attitude to be exemplified daily with standard work.
Outstanding team dynamics and idea generation are promoted.
How will you get here? Education Bachelor's degree in chemical engineering (or other engineering field), chemistry, pharmacy, or another related science or technical field is required.
Experience
Minimum of one (1) to three (3) years of experience in a manufacturing environment preferred.
Experience in product or process development, including scale‑up and technology transfer processes for both immediate and controlled release dosage forms preferred.
Project Management experience preferred.
Knowledge, Skills, Abilities
Understanding of Good Manufacturing Practices (GMP) and regulatory compliance.
Lead projects of moderate to high complexity in scope and compliance‑related challenges to implement processes that meet changing regulations.
Proficiency using Microsoft (MS) Office applications.
Good critical and logical thinking skills. Effective written, interpersonal, and presentation skills, including leading technical discussions with internal and external clients.
Self‑starter, mature, independent, and detail oriented.
Ability to work in a fast‑paced, results‑oriented, and structured environment.
Experience leading projects related to process development, including scale‑up production activities.
Effective time management, multi‑tasking, and tracing skills to run multiple projects.
Lead by example.
Courages and assumes challenges in a risk‑based approach.
Transparent and knowledgeable in presenting project updates daily.
Diligent in team meetings and discussions.
Collaborate across multiple departments to reach goals and objectives.
Inclusive communication styles and ideas.
Conscientious toward fellow peers and work‑load requirements.
Coordinate and lead weekly meetings with customers.
Fast and focused execution of tasks will be required at times.
Build helpful ideas to increase production efficiencies.
Transfer technical skill information to supporting departments.n Participate and support audit participation and interaction for regulatory agencies.
Develop and transform learning for peers with technical and mechanical result‑oriented aptitudes.
Written communication skills expected, and presentation will be expected.
Equivalent combinations of education, training, and meaningful work experience may be considered.
Physical Requirements Position requires ordinary ambulatory skills and physical coordination sufficient to move around office and manufacturing locations; ability to stand, walk, stoop, kneel, crouch periodically, and manipulate light to medium weights (10–35 pounds). Requires arm, hand, and finger dexterity, including the ability to type for periods of time; visual acuity to use a keyboard, computer monitor, operate equipment, and read materials; ability to sit, reach with hands and arms, talk, and hear for prolonged periods.
zny- The Thermo Fisher team of 100,000 outstanding minds invites you to join and help enable our customers to make the world healthier, cleaner, and safer.
Apply today:
http://jobs.thermofisher.com
Thermo Fisher Scientific is an EEO Spielautomaten and affirmative action employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status.
#J-18808-Ljbffr