Top 78 Author Jobs in South Carolina

Sr. Process Engineer
Alcami Corporation —Charleston, SC
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Ability to walk for extended periods
Application Engineer - Fuel Injection
ilocatum —Greenville, SC
- $95,000 - $125,000 a year
- Full-time
- 5 years
- Office
- Analysis skills
- Health insurance
- Dental insurance
Quick Apply
2d
Executive Chef Manager
Corporate Dining Concepts —North Charleston, SC
- $60,000 - $70,000 a year
- Full-time
- ServSafe
- Cooking
- 3 years
- Health insurance
- Dental insurance
Quick Apply
12d
IT Policy Analyst
SMS DATA PRODUCTS GROUP, INC —Shaw AFB, SC
- Full-time
- 5 years
- Bachelor of Science
- Public speaking
- Opportunities for advancement
Quick Apply
QA Coordinator
The Ritedose Corporation —Columbia, SC
- $26 - $29 an hour
- Microsoft Excel
- Microsoft Outlook
- Laboratory experience
Quick Apply
10d
Sr. Communications Manager - Science Media Relations
American Heart Association —Charleston, SC
- $86,000 - $102,000 a year
- Full-time
- Remote
- Microsoft Excel
- 3 years
- Supervising experience
- Wellness program
- Paid holidays
5d
Principal Consultant- Provider Affiliation and Optimization
SullivanCotter, Inc. —South Carolina
- $217,000 - $325,600 a year
- Full-time
- Remote
- Word processing
- 11+ years
- Master's degree
- Profit sharing
- AD&D insurance
Technical Writer
TIAG —Mount Pleasant, SC
- $55,000 - $65,000 a year
- Full-time
- Mid-level
- Office
- Analysis skills
Quick Apply
Intelligence Planner
Credence —Shaw AFB, SC
- Full-time
- 6 years
- Analysis skills
- Bachelor's degree
- AD&D insurance
- Disability insurance
Quick Apply
10d
Administrative Professional
Ted Law Firm —North Charleston, SC
- Mid-level
- High school diploma or GED
- Data entry
- Opportunities for advancement
Quick Apply
Clinical Scientist - Ophthalmology
サイネオス・ヘルス —South Carolina
- Remote
- Mid-level
- Employee stock purchase plan
- Health insurance
Principal Software Engineer
CVS Health —South Carolina
- $144,200 - $288,400 a year
- Full-time
- Remote
- Oracle
- High school diploma or GED
- Bachelor's degree
- Health insurance
- Dental insurance
12d
Clinical Scientist - Cardiovascular
サイネオス・ヘルス —South Carolina
- Remote
- Mid-level
- Cardiology
- Employee stock purchase plan
- Health insurance
Clinical Scientist - Respiratory
サイネオス・ヘルス —South Carolina
- Remote
- Mid-level
- Employee stock purchase plan
- Health insurance
Primary Packaging Operations Associate
NEPHRON SC, LLC —West Columbia, SC
- Writing skills
- Mid-level
- Office
Security Design Project Engineer 1 - Charleston, SC
M.C. Dean, Inc —Charleston, SC
- Full-time
- Computer Science
- Mid-level
- Bachelor's degree
System Specialist, Associate
M.C. Dean, Inc —Rock Hill, SC
- Full-time
- Mid-level
- SQL
- Presentation skills
Clinical Scientist - Immunology (Expertise in Ulcerative Colitis, Crohn’s disease and Rheumatology + Excel) - Clinical Drug Trial Exp - Must Have
サイネオス・ヘルス —South Carolina
- Remote
- Senior level
- Employee stock purchase plan
- Health insurance
Commercial Lead
HNTB Corporation —North Charleston, SC
- Full-time
- Engineering
- Office
- Analysis skills
Plant Manager
Meyer Utility Structures, LLC —Lancaster, SC
- 11+ years
- Bachelor's degree
- Recruiting
Quick Apply

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author jobs near south carolina

Sr. Process Engineer

Alcami Corporation -
Charleston, SC

Apply Now

Job Details

Full-time

Qualifications

Customer communication
Microsoft Excel
Microsoft Outlook
Word embeddings
Manufacturing facility experience
Pharmaceutical company experience
Pharmaceutical manufacturing facility experience

Full Job Description

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?

Job Summary:

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.

On-Site Expectations:

100% on-site position.
1st Shift: Monday - Friday, 8:00am - 5:00pm.

Responsibilities:

Provides technical assistance for process tech transfer and validation efforts for assigned manufacturing projects.
Writes Master Batch Records with a strong understanding of equipment, critical process parameters, in-process tests, etc.
Monitors manufacturing processes during production runs to assess any technical process issues and provides troubleshooting support as needed.
Author manufacturing investigations and complete CAPA assignments.
Composes process validation documentation, including CQA assessment, pFMEA risk assessment, and process validation protocols.
Identifies specific parameters, sampling, and tests used in the validation protocols of new and existing products.
Interact with clients during routinely scheduled project meetings.
Ensures timely completion and compliance with cGMP and all other relevant company training requirements.
Other duties as assigned.

Qualifications:

Bachelor’s degree in Engineering, Pharmacy, or Chemistry.
5 years of experience of technical support in a sterile pharmaceutical manufacturing environment.
Previous experience supporting tech transfer of parenteral Drug Products preferred.

Knowledge, Skills, and Abilities:

Excellent verbal communication, written communication, documentation, negotiation, critical thinking, analytical, problem solving, detail orientation, organization and time management skills required.
Working knowledge of cGMP requirements related to sterile Drug Product manufacturing processes.
Working knowledge of EU regulations preferred.
Proficiency with Microsoft office (Word, Excel, Outlook) required.
Ability to interact with internal stakeholders and external customers.

Travel Expectations:

Up to 5% domestic travel.

Physical Demands and Work Environment:

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.

#IND1

Apply Now

Refine Your Search

author jobs in south carolina

Sr. Process Engineer

Application Engineer - Fuel Injection

Executive Chef Manager

IT Policy Analyst

QA Coordinator

Sr. Communications Manager - Science Media Relations

Principal Consultant- Provider Affiliation and Optimization

Technical Writer

Intelligence Planner

Administrative Professional

Clinical Scientist - Ophthalmology

Principal Software Engineer

Clinical Scientist - Cardiovascular

Clinical Scientist - Respiratory

Primary Packaging Operations Associate

Security Design Project Engineer 1 - Charleston, SC

System Specialist, Associate

Clinical Scientist - Immunology (Expertise in Ulcerative Colitis, Crohn’s disease and Rheumatology + Excel) - Clinical Drug Trial Exp - Must Have

Commercial Lead

Plant Manager

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